The present invention relates to a method for preparing an amino salt compound comprising: i) providing a carbonyl compound; ii) reacting the carbonyl compound provided according to (i) in the presence of a transaminase with ii-a) at least one primary amine; and ii-b) at least one carboxylic acid; thereby obtaining a mixture comprising an at least partially crystallized amino salt compound comprising an amino cation and a carboxylate anion based on the at least one carboxylic acid added according to (ii-b).

Biotransformations became over the past decades a powerful technique for the synthesis of valuable compounds on laboratory and industrial scale. Herein pyridoxal 5’-phosphate (PLP)- dependent transaminases (TAs) and especially amine transaminases (AT As) have gained in recent years a significant impact in the synthesis of optically pure amines, which are valuable building blocks for various agrochemicals and active pharmaceutical ingredients, e.g. sitagliptin. These enzymes basically catalyze the deamination of a primary amine (amine donor) with a simultaneous amination of an aldehyde or ketone (amine acceptor). The transamination- reaction can be carried out as a kinetic resolution of a racemic amine or an asymmetric synthesis from the respective prochiral ketone. Due to a maximum yield of 100% the

asymmetric synthesis is in theory preferred, especially if a catalyst with high enantioselectivity is used. Unfortunately thermodynamic limitations and certain product inhibitions tend to limit the applicability of transaminases in asymmetric synthesis, which needs to be overcome for synthetic purposes. Aside using an uneconomic excess of the amine donor, complex

(co-)product removal techniques are currently considered, e.g. enzymatic cascades, membrane processes and non-catalytic side reactions. Such techniques unfortunately always increase (in general) overall complexity of the biocatalytic reaction systems, require additional or tailor-made co-substrates and generate further by-products.

The object of the present invention was therefore the provision of a method for the preparation of a desired product amine via biotransformation, especially using a transaminase, which overcomes the above-mentioned drawbacks.

The object was solved by a method for preparing an amino salt compound comprising:

i) providing a carbonyl compound of general formula (I)

wherein

R ¹ is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20- alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4-C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20- cycloalkinyl, C5-C20-aryl, C6-C20-alkylaryl, C6-C20-arylalkyl, C2-C20- heteroalkyl, C3-C20-cyclic heteroalkyl, C4-C20-heteroaryl, C5-C20- alkylheteroaryl and C5-C20-heteroarylalkyl, wherein in case of more than one (hetero)aliphatic or (hetero)aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy; and R ² is selected from the group consisting of hydrogen atom, branched or unbranched C1-C5-alkyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C5-C10-aryl, C6-C10-alkylaryl and C6-C10-arylalkyl, wherein in case of more than one aromatic ring system the ring systems are condensed or separate, wherein each residue R ² has at least one substituent R ^2a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy; or

R ¹ , R ² together form a C3-C10-cycloalkyl or C3-C10-cycloalkenyl, wherein the C3-C10- cycloalkyl or C3-C10-cycloalkenyl each has at least one substituent R ^x selected from the group consisting of hydrogen atom, C1-C5-alkyl, C1-C4-heteroalkyl and C1-C5-alkyl-R ^y , wherein R ^y is hydroxyl or thiol;

ii) reacting the carbonyl compound provided according to (i) in the presence of a

transaminase with

ii-a) at least one primary amine; and

ii-b) at least one carboxylic acid;

thereby obtaining a mixture comprising an at least partially crystallized amino salt compound comprising

a cation of general formula (II)

wherein R ¹ and R ² are as defined for general formula (I) and

a carboxylate anion based on the at least one carboxylic acid added according to (ii- b).

The expression“amino salt compound” comprises cation and anion as described above. The amino salt compound can be present as pure salt compound (unsolvated, anhydrated) or as solvate or hydrate or mixture thereof, wherein hydrate includes hemihydrate, monohydrate and polyhydrate and solvate includes hemisolvate, monosolvate and polysolvate.“At least partially crystallized” means that at least 50%, preferably at least 60%, more preferably at least 70%, more preferably at least 80%, more preferably at least 90% of the amine salt compound precipitate in crystalline form. The wording“hetero” means that heteroatom(s) are present, which are selected from the group consisting of nitrogen atom, sulphur atom and oxygen atom, if not otherwise indicated. The heteroatom(s) is/are present as members of the respective chain or ring structure. The residues R ^1a · ^2a are as defined above. It has to be noted that neither R ^1a nor R ^2a is a substituent which comprises a charge, i.e., substituents having a charge are excluded as R ^1a and as R ^2a . For example, R ^1a and also R ^2a are no carboxyl/carboxylate, no phosphate, no sulfonate. In a preferred embodiment, the combination of R ¹ , R ^1a being a perfluorinated alkyl is excluded. The same applies for R ² and R ^2a , i.e. the combination of R ² and R ^2a being a perfluorinated alkyl is excluded as well. In other words, neither the combination of R ¹ and R ^1a nor the combination of R ² and R ^2a is a perfluorinated alkyl. Regarding the embodiment wherein R ¹ and R ² together form a C3-C10-cycloalkyl or a C3-C10- cycloalkenyl, the number of C atoms indicated includes the carbonyl C atom situated between R ¹ and R ² .

With this method as described above, the inventors now present a crystallization-based approach for the direct removal of the desired product amine from a transaminase-catalyzed reaction. Scheme 1 shows the method based on the exemplarily product amine

1-phenylethylamine. The product amine 2 is herein selectively crystallized from solution as a barely soluble amine salt 6, while all other reactants, especially the applied donor amine (isopropyl amine, 3), remains in solution. This in situ-product crystallization (ISPC) continuously removes the desired product amine from solution and thus yields an equilibrium displacement towards the products. The counter ion (here shown as a carboxylate) is added directly to the reaction solution and can be isolated for reuse from the formed solid salt. A stoichiometric use of the carboxylate in comparison to the applied amines is not required (see below).

Scheme 1 : Combination of an in situ-product crystallization (ISPC) with a transaminase- catalyzed reaction to yield a barely soluble 1-phenylethylamine salt; shown protonation of reactants are based on an aqueous solution at pH 7.5; TA = transaminase, PLP = pyridoxal 5’-phosphate, R = exemplary residue representing a suitable carbon containing residue.

First, the main requirement of this concept is the choice of a specific counter ion, i.e. a specific carboxylic acid, which generates a barely soluble salt with the target amine for its crystallization, while the donor amine salt is not crystallized. Unfortunately, most commonly used amine salts, especially amine halide salts, show very high solubilities in aqueous solutions and thus are not applicable for such an ISPC concept. Thus, a preferred embodiment of the method is that the amino salt compound obtained according to (ii) has a solubility in water at pH 7 which is smaller than the solubility in water of the at least one primary amine added according to (ii-a). A further preferred embodiment of the method is that the amino salt compound obtained according to (ii) has a solubility in water at pH 7≤ 30 mmol/l, preferably≤ 25 mmol/l, more preferably≤ 10 mmol/l.

According to a preferred embodiment, the solubility difference (deltas _oi. ) between the solubility of the salt of the primary amine and the solubility of the amino salt compound is at least 10 mmol/l. As explained above, the solubility of the salt of the primary amine (sol. p _{rimary amine salt} ) is higher than the solubility of the amino salt compound i.e.:

Second, the used transaminase has to tolerate the required concentration of the chosen compound. Third, the formed salt has to be stable under process conditions and should be easily recovered from the reaction mixture.

Carboxylic acid

According to step (ii), the carbonyl compound provided according to (i) is reacted in the presence of a transaminase with ii-a) at least one primary amine; and ii-b) at least one carboxylic acid.

Regarding the carboxylic acid to be used for (ii-b), commercially readily available aliphatic, aromatic and heteroaromatic carboxylic acids (R-COOH) were selected and screened as their respective carboxylate salts towards common amines from a transaminase-catalyzed reaction. 1-phenylethylamine and substituted derivatives 2a-f thereof served as model product amines and were compared with typical donor amines such as isopropylamine 3, racemic 2-butylamine, DL-alanine and L-alanine (see Example section for further details). Here the salt of the product amine needs to exhibit a significant lower solubility then its donor amine salt counterpart since the donor amine is still applied with an excess.

Preferably, the at least one carboxylic acid according to (ii-b) is used in its protonated form or in deprotonated form with a suitable counter cation. The above-described straight-forward screening approach resulted in the finding, that the at least one carboxylic acid according to (ii- b) is preferably a carboxylic acid of general formula (III)

wherein n is zero or 1 ;

the residues R ³ and R ⁴ are both phenyl or together form a phenyl ring, wherein each phenyl ring has at least one further substituent selected from the group consisting of hydrogen atom, halogen atom, preferably chloro, and nitro group; and the residue R ⁵ is hydrogen atom or methyl or absent if R ³ and R ⁴ together form a phenyl ring. The straight-forward screening approach especially resulted in two benzylbenzene-based acids and three benzoic acid derivatives that matched the above mentioned criteria (as the respective carboxylate ions at pH 7.5) (Scheme 2).

Scheme 2: Potential carboxylic acids and the abbreviations used for an in situ product

crystallization of amines from a transaminase-catalyzed reaction.

In addition, 2,2-diphenylpropionic acid (2DPPA) was identified as suitable carboxylic acid. Thus, a preferred embodiment of the method relates to the at least one carboxylic acid according to (ii-b) being a carboxylic acid selected from the group consisting of diphenylacetic acid (DPAA), 2,2-diphenylpropionic acid (2DPPA), 3,3-diphenylpropionic acid (3DPPA), 3,4-dichloro-benzoic acid (34CA), 3,4-dinitro-benzoic acid (34NA) and 4-chloro-3-nitro-benzoic acid (43CNA). More preferably, the at least one carboxylic acid according to (ii-b) is selected from the group consisting of diphenylacetic acid (DPAA), 2,2-diphenylpropionic acid (2DPPA) and 3,3- diphenylpropionic acid (3DPPA), more preferably 2,2-diphenylpropionic acid (2DPPA) or 3,3- diphenylpropionic acid (3DPPA), more preferably at least 3DPPA.

Carbonyl compound

According to step (i), a carbonyl compound of general formula (I) is provided. Preferably,

R ¹ is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4- C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, C6-C20- alkylaryl, C6-C20-arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, C4-C20- heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl, wherein in case of more than one (hetero)aliphatic or (hetero)aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy; and R ² is selected from the group consisting of hydrogen atom, branched or unbranched C1-C5- alkyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1- C10-alkoxy, C5-C10-aryl, C6-C10-alkylaryl and C6-C10-arylalkyl, wherein in case of more than one aromatic ring system the ring systems are condensed or separate, wherein each residue R ² has at least one substituent R ^2a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy.

More preferably, the residue R ¹ is selected from the group consisting of branched or

unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4-C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, C6- C20-alkylaryl, C6-C20-arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, C4-C20- heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl, wherein the hetero atom(s) in C4-C20-heteroaryl, C5-C20-a I kyl heteroaryl and C5-C20-heteroarylalkyl is/are oxygen or sulfur and the hetero atom(s) in C2-C20-heteroalkyl and C3-C20-cyclic heteroalkyl, is/are selected from oxygen, sulfur and nitrogen, wherein in case of more than one (hetero)aliphatic or

(hetero)aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy.

According to a preferred embodiment of the method, the residue R ¹ is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4-C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20- cycloalkinyl, C5-C20-aryl, C6-C20-alkylaryl, C6-C20-arylalkyl, C2-C20-heteroalkyl, C3-C20- cyclic heteroalkyl, wherein the hetero atom(s) is/are selected from oxygen, sulfur and nitrogen wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy. According to a further preferred embodiment of the method, the residue R ¹ is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, C4-C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl and C5-C20-aryl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy.

According to a more preferred embodiment of the method, the residue R ¹ is selected from the group consisting of branched or unbranched C2-C10-alkyl, C5-C10-cycloalkyl and C5-C20-aryl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy; R ¹ being preferably selected from the group consisting of methyl, iso-propyl, cyclohexyl and phenyl, wherein phenyl has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom, preferably fluoro or chloro, and methoxy, preferably meta- or para- methoxy.

For R ¹ being branched or unbranched C2-C20-alkyl or branched or unbranched C2-C20- alkenyl, a preferred embodiment relates to R ¹ being branched or unbranched C4-C20-alkyl or branched or unbranched C4-C20-alkenyl.

According to a preferred embodiment of the method, the residue R ² is selected from the group consisting of hydrogen atom, branched or unbranched C1-C5-alkyl, wherein each residue R ² has at least one substituent R ^2a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy. According to a further preferred embodiment of the method, the residue R ² is selected from the group of branched or unbranched C1-C3-alkyl, R ² being preferably methyl.

Transaminase

According to step (ii), the carbonyl compound provided according to (i) is reacted in the presence of a transaminase. Preferably, the transaminase according to (ii) is selected from the group of transaminases, preferably from the group of amine transaminases, more preferably selected from the group consisting of amine transaminase from Aspergillus fumigates (AfATA) according to SEQ ID NO 1 , amine transaminase from Gibberella zeae (GzATA) according to SEQ ID NO 2, amine transaminase from Neosartorya fischeri (NfATA) according to SEQ ID NO 3, amine transaminase from Aspergillus oryzae (AoATA) according to SEQ ID NO 4, amine transaminase from Aspergillus terreus (AtATA) according to SEQ ID NO 5, amine transaminase from Mycobacterium vanbaalenii (MvATA) according to SEQ ID NO 6, amine transaminase from Silicibacter pomeroyi (SpATA) according to SEQ ID NO 7 and a homologue enzyme having sequence identity of at least 65% with any one of SEQ ID NO 1 to 7 and having the same function as the amine transaminase of SEQ ID NO 1 to 7, more preferably selected from the group consisting of the amine transaminase from Mycobacterium vanbaalenii (MvATA) according to SEQ ID NO 6, the amine transaminase from Silicibacter pomeroyi (SpATA) according to SEQ ID NO 7 and a homologue enzyme having sequence identity of at least 65% with any one of SEQ ID NO 6 or 7 and having the same function as the amine transaminase of SEQ ID NO 6 or 7. Table 1 shows an overview of the preferred amine transaminases:

Table 1: Amine transaminases of SEQ ID Nos 1 to 7

The expression“having the same function as the amine transaminase of any one of SEQ ID NO. 1 to 7” means that the homologue enzyme catalyzes an amine transaminase reaction at least with an effectivity of 90% as the transaminase of any one of SEQ ID NO. 1 to 7.

Preferably, the homologue enzyme has a sequence identity of at least 75%, preferably at least 85%, more preferably at least 90%, more preferably at least 95%, more preferably at least 98%, more preferably at least 99%, with any one of SEQ ID NO 1 to 7 and has the same function as the amine transaminase of SEQ ID NO 1 to 7.

Primary amine

According to step (ii), the carbonyl compound provided according to (i) is reacted in the presence of a transaminase with ii-a) at least one primary amine; and ii-b) at least one carboxylic acid. Preferably, the at least one primary amine according to (ii-a) is used in non- protonated form or in protonated form with a suitable counter anion.

According to a preferred embodiment of the method, the at least one primary amine according to (ii-a) is selected from the group of mono- and diamines having one to 10 carbon atoms, preferably from the group consisting of 1 ,5-diamino-pentane (cadaverine), alanine, 2-amino- butane (sec-butylamine) and 2-amino-propane, and is preferably 2-amino-propane (iso- propylamine) in its non-protonated or protonated form, wherein the protonated form is present in combination with a suitable anion.

According to a more preferred embodiment of the method, the at least one primary amine according to (ii-a) and the at least one carboxylic acid according to (ii-b) are used as one or more salt(s) comprising the protonated form of the at least one primary amine and the deprotonated form of the at least one carboxylic acid, preferably as one salt comprising the protonated form of the at least one primary amine and the deprotonated form of the at least one carboxylic acid, more preferably as isopropyl ammonium 3,3-diphenylpropionate.

Amino salt compound

According to step (ii), an amino salt compound is obtained. Preferably, the amino salt compound obtained according to (ii) comprises a cation of general formula (II)

wherein R ¹ and R ² are as defined for general formula (I), and an anion based on the at least one carboxylic acid, which is preferably an anion of general formula (Ilia)

wherein n is zero or 1 ;

the residues R ³ and R ⁴ are both phenyl or together form a phenyl ring, wherein each phenyl ring has at least one further substituent selected from the group consisting of hydrogen atom, halogen atom, preferably chloro, and nitro group and the residue R ⁵ is hydrogen atom or methyl or absent if R ³ and R ⁴ together form a phenyl ring; wherein the anion of general formula (Ilia) is preferably selected from the group consisting of diphenylacetate, 2,2-diphenylpropionate, 3,3- diphenylpropioniate, 3,4-dichloro-benzoate, 3,4-dinitro-benzoate and 4-chloro-3-nitro-benzoate, more preferably form the group consisting of diphenylacetate, 2,2-diphenylpropionate, 3,3- diphenylpropioniate, more preferably 2,2-diphenylpropionate or 3,3-diphenylpropionate, more preferably 3,3-diphenylpropionate.

Further reaction conditions

According to a preferred embodiment of the method, the reaction according to (ii) is carried out in an aqueous solution, which preferably comprises at least 80 weight-%, more preferably at least 90 weight-%, more preferably at least 95 weight-%, more preferably at least 98 weight-%, water, based on the overall weight of the aqueous solution. The aqueous solution preferably comprises a buffer, preferably selected from the group of tris(hydroxymethyl)aminomethane buffer (TRIS buffer), 3-(N-morpholino)propanesulfonic acid buffer (MOPS buffer), N,N-Bis(2- hydroxyethyl)-2-aminoethanesulfonic acid buffer (BES buffer), N-(tris(hydroxymethyl)methyl)- glycine buffer (Tricine buffer), Carbonate buffer, N-cyclohexyl-2-aminoethanesulfonic acid buffer (CHES buffer), 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid buffer (HEPES buffer) and phosphate buffer, more preferably at least a phosphate buffer. According to further a preferred embodiment of the method, the reaction according to (ii) is carried out at a pH value in the range of 6.0 to 9.5, more preferably in the range of from 6.5 to 9.0, more preferably in the range of from 7.0 to 8.0. According to a further preferred

embodiment of the method, the reaction according to (ii) is carried out for a time period of at least one hour, more preferably for a time in the range of from 1 to 1 ,000 hours, more preferably in the range of from 5 to 500 hours, more preferably in the range of from 10 to 200 hours.

According to a further preferred embodiment of the method, the reaction according to (ii) is carried out at a temperature in the range of from 10 to 50 °C, more preferably in the range of from 15 to 45 °C, more preferably in the range of from 20 to 40 °C, more preferably in the range of from 25 to 35 °C.

According to another preferred embodiment of the method, for the at least one carboxylic acid being a carboxylic acid according to general formula (III), wherein the residues R ³ and R ⁴ together form a phenyl ring, preferably a carboxylic acid selected from the group consisting of 3,4-dichloro-benzoic acid (34CA), 3,4-dinitro-benzoic acid (34NA) and 4-chloro-3-nitro-benzoic acid (43CNA), the concentration of the at least one carboxylic acid is kept in the range of from 0.001 to 50 mM, preferably in the range of from 1 to 45 mM, more preferably in the range of from 5 to 40 mM during step (ii). According to another preferred embodiment of the method, for the at least one carboxylic acid being a carboxylic acid according to general formula (III), wherein the residues R ³ and R ⁴ are each a phenyl ring, preferably a carboxylic acid selected from the group consisting of diphenylacetic acid (DPAA), 2,2-diphenylpropionic acid (2DPPA) and 3,3-diphenylpropionic acid (3DPPA), the concentration of the at least one carboxylic acid is ≤50 mM during step (ii).

Further reaction steps

As described above, the method comprises reaction steps (i) and (ii). According to a preferred embodiment, the method further comprises:

iii) separating the at least partially crystallized amine salt compound obtained according to (ii) from the mixture thereby obtaining the crystallized amine salt compound.

Preferably, separating the crystallized amine salt compound according to (iii) from the mixture is done by sedimentation, centrifugation or filtration, preferably by filtration.

According to a further preferred embodiment, the method further comprises, preferably in addition to (i), (ii) and (iii):

(iv) optionally washing the separated crystallized amino salt compound obtained according to (iii), preferably with water or an organic solvent or a mixture thereof, more preferably with water or methyl tert-butyl ether or a mixture thereof, thereby obtaining a washed crystallized amino salt compound;

(v) dissolving the crystallized amino salt compound obtained according to (iii) or optionally the washed crystallized amino salt compound obtained according to (iv) in an aqueous solution having a pH value in the range of from 10 to 14 comprising at least one base, preferably a base comprising a hydroxide ion, thereby obtaining an aqueous solution comprising an amine of general formula (I la)

wherein R ¹ and R ² are as defined for general formula (I);

(vi) extracting the aqueous solution obtained according to (v) at least once with a water

immiscible organic solvent obtaining an organic phase comprising at least parts of the amine of general formula (I la); and an aqueous phase comprising at least parts of the anion of general formula (Ilia)

wherein n is zero or 1 ; and wherein the residues R ³ and R ⁴ are both phenyl or together form a phenyl ring, wherein each phenyl ring has at least one further substituent selected from the group consisting of hydrogen atom, halogen atom, preferably chloro, and nitro group and the residue R ⁵ is hydrogen atom or methyl or absent if R ³ and R ⁴ together form a phenyl ring; wherein the anion of general formula (Ilia) is preferably selected from the group consisting of diphenylacetate, 2,2-diphenylpropionate, 3,3- diphenylpropionate, 3,4-dichloro-benzoate, 3,4-dinitro-benzoate and 4-chloro-3-nitro- benzoate, more preferably from the group consisting of diphenylacetate, 2,2- diphenylpropionate, 3,3-diphenylpropionate, more preferably 2,2-diphenylpropionate or 3,3-diphenylpropionate, more preferably 3,3-diphenylpropionate.

The water immiscible organic solvent according to (vi) has preferably a Kow value of at least 0.5, more preferably of at least 0.6, more preferably of at least 0.7, more preferably of at least 0.8. According to a preferred embodiment, the water immiscible organic solvent according to (vi) is selected from the group of ethers, more preferably from the group of aliphatic ethers, more preferably MTBE (methyl-tert-butylether).

According to a further preferred embodiment, the method further comprises, preferably in addition to (i), (ii), (iii), (iv), (v) and (vi):

(vii-a) removal of the water immiscible organic solvent from the organic phase obtained in (vi) thereby obtaining the amine of general formula (I la),

wherein R ¹ and R ² are as defined for general formula (I).

According to an alternative preferred embodiment, the method further comprises, preferably in addition to (i), (ii), (iii), (iv), (v) and (vi): (vii-b) adding at least one acid HX to the organic phase obtained according to (vi), preferably HCI, thereby obtaining a salt of general formula (IV)

wherein R ¹ and R ² are as defined for general formula (I) and (II) and X is an ion based on the at least one acid HX, preferably Cl.

According to an alternative preferred embodiment, the method further comprises, preferably in addition to (i), (ii), (iii), (iv), (v), (vi) and (vii-a) or in addition to (i), (ii), (iii), (iv), (v), (vi) and (vii-b): (viii) optionally precipitating the at least one carboxylic acid of general formula (III)

wherein

n is zero or 1 ;

the residues R ³ and R ⁴ are both phenyl or together form a phenyl ring, wherein each phenyl ring has at least one further substituent selected from the group consisting of hydrogen atom, halogen atom, preferably chloro, and nitro group and the residue R ⁵ is hydrogen atom or methyl or absent if R ³ and R ⁴ together form a phenyl ring; preferably the at least one carboxylic acid being selected from the group consisting of

diphenylacetic acid (DPAA), 2,2-diphenylpropionic acid (2DPPA), 3,3-diphenylpropionic acid (3DPPA), 3,4-dichloro-benzoic acid (34CA), 3,4-dinitro-benzoic acid (34NA) and 4- chloro-3-nitro-benzoic acid (43CNA), more preferably form the group consisting of diphenylacetic acid (DPAA), 2,2-diphenylpropionic acid (2DPPA) and 3,3- diphenylpropionic acid (3DPPA), more preferably 2,2-diphenylpropionic acid (2DPPA) or 3,3-diphenylpropionic acid (3DPPA), more preferably at least 3DPPA,

from the aqueous phase obtained according to (vi) by adjusting the pH to a value in the range of from 0 to 6, preferably by addition of HCI, and

(ix) optionally recycling the at least one carboxylic acid precipitated according to (viii) to the process, preferably to step (ii).

The present invention also relates to an amino salt compound obtained or obtainable by the method as described above.

In another aspect, the present invention relates to an amino salt compound comprising

a cation of general formula (II)

wherein

R ¹ is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20- alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4-C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20- cycloalkinyl, C5-C20-aryl, C6-C20-alkylaryl, C6-C20-arylalkyl, C2-C20- heteroalkyl, C3-C20-cyclic heteroalkyl, C4-C20-heteroaryl, C5-C20- alkylheteroaryl and C5-C20-heteroarylalkyl, wherein in case of more than one (hetero)aliphatic or (hetero)aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy; and R ² is selected from the group consisting of hydrogen atom, branched or unbranched C1-C5-alkyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C5-C10-aryl, C6-C10-alkylaryl and C6-C10-arylalkyl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ² has at least one substituent R ^2a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy; or

R ¹ , R ² together form a C3-C10-cycloalkyl or C3-C10-cycloalkenyl, wherein the C3-C10- cycloalkyl or C3-C10-cycloalkenyl each has at least one substituent R ^x selected from the group consisting of hydrogen atom, C1-C5-alkyl, C1-C4-heteroalkyl and C1-C5-alkyl-R ^y , wherein R is hydroxyl or thiol; and

an anion of general formula (Ilia)

wherein

n is zero or 1 ;

the residues R ³ and R ⁴ are both phenyl or together form a phenyl ring, wherein each phenyl ring has at least one further substituent selected from the group consisting of hydrogen atom, halogen atom, preferably chloro, and nitro group and the residue R ⁵ is hydrogen atom or methyl or absent if R ³ and R ⁴ together form a phenyl ring.

Preferably, the anion of general formula (Ilia) of the amine salt compound is selected from the group consisting of diphenylacetate, 2,2-diphenylpropionate, 3,3-diphenylpropionate, 3,4- dichloro-benzoate, 3,4-dinitro-benzoate and 4-chloro-3-nitro-benzoate, more preferably from the group consisting of diphenylacetate, 2,2-diphenylpropionate, 3,3-diphenylpropionate, more preferably 2,2-diphenylpropionate or 3,3-diphenylpropionate, more preferably 3,3- diphenylpropionate.

According to a preferred embodiment of the amino salt compound,

R ¹ is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4- C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, C6-C20- alkylaryl, C6-C20-arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, C4-C20- heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl, wherein in case of more than one (hetero)aliphatic or (hetero)aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy; and R ² is selected from the group consisting of hydrogen atom, branched or unbranched C1-C5- alkyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1- C10-alkoxy, C5-C10-aryl, C6-C10-alkylaryl and C6-C10-arylalkyl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ² has at least one substituent R ^2a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy.

More preferably, the residue R ¹ is selected from the group consisting of branched or

unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4-C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, C6- C20-alkylaryl, C6-C20-arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, C4-C20- heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl, wherein the hetero atom(s) in C4-C20-heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl is/are oxygen or sulfur and the hetero atom(s) in C2-C20-heteroalkyl and C3-C20-cyclic heteroalkyl, is/are selected from oxygen, sulfur and nitrogen, wherein in case of more than one (hetero)aliphatic or

(hetero)aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy. According to a further preferred embodiment of the amino salt compound, the residue R ¹ is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4-C20- cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, C6-C20-alkylaryl, C6-C20- arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy. According to a further preferred embodiment of the amino salt compound, the residue R ¹ is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, C4-C20- cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy. According to a further preferred

embodiment of the amino salt compound, the residue R ¹ is selected from the group consisting of branched or unbranched C2-C10-alkyl, C5-C10-cycloalkyl and C5-C20-aryl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy; R ¹ being preferably selected from the group consisting of methyl, iso-propyl, cyclohexyl and phenyl, wherein phenyl has at least one substituent selected from the group consisting of hydrogen atom, halogen atom, preferably fluoro or chloro, and methoxy, preferably meta- or para-methoxy.

For R ¹ being branched or unbranched C2-C20-alkyl or branched or unbranched C2-C20- alkenyl, a preferred embodiment relates to R ¹ being branched or unbranched C4-C20-alkyl or branched or unbranched C4-C20-alkenyl.

According to a preferred embodiment of the amino salt compound, the residue R ² is selected from the group consisting of hydrogen atom, branched or unbranched C1-C5-alkyl, wherein each residue R ² has at least one substituent R ^2a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy. Preferably, the residue R ² is selected from the group consisting of branched or unbranched C1-C3-alkyl, R ² being preferably methyl.

In a preferred embodiment, the combination of R ¹ , R ^1a being a perfluorinated alkyl is excluded. The same applies for R ² and R ^2a , i.e. the combination of R ² and R ^2a being a perfluorinated alkyl is excluded as well. In other words, neither the combination of R ¹ and R ^1a nor the combination of R ² and R ^2a is a perfluorinated alkyl.

Regarding the embodiment wherein R ¹ and R ² together form a C3-C10-cycloalkyl or a C3-C10- cycloalkenyl, the number of C atoms indicated includes the carbonyl C atom situated between R ¹ and R ² .

The present invention in another aspect relates to a composition comprising

a) an amine of general formula (I la) wherein

R ¹ is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20- alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4-C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20- cycloalkinyl, C5-C20-aryl, C6-C20-alkylaryl, C6-C20-arylalkyl, C2-C20- heteroalkyl, C3-C20-cyclic heteroalkyl, C4-C20-heteroaryl, C5-C20- alkylheteroaryl and C5-C20-heteroarylalkyl, wherein in case of more than one (hetero)aliphatic or (hetero)aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy; and

R ² is selected from the group consisting of hydrogen atom, branched or unbranched C1-C5-alkyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C5-C10-aryl, C6-C10-alkylaryl and C6-C10-arylalkyl, wherein in case of more than one aromatic ring system the ring systems are condensed or separate, wherein each residue R ² has at least one substituent R ^2a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy; or

R ¹ , R ² together form a C3-C10-cycloalkyl or C3-C10-cycloalkenyl, wherein the C3-C10- cycloalkyl or C3-C10-cycloalkenyl each has at least one substituent R ^x selected from the group consisting of hydrogen atom, C1-C5-alkyl, C1-C4-heteroalkyl and C1-C5-alkyl-R ^y , wherein R ^y is hydroxyl or thiol;

and

b) at least one carboxylic acid of general formula (III)

wherein

n is zero or 1 ;

the residues R ³ and R ⁴ are both phenyl or together form a phenyl ring, wherein each phenyl ring has at least one further substituent selected from the group consisting of hydrogen atom, halogen atom, preferably chloro, and nitro group; and the residue R ⁵ is hydrogen atom or methyl or absent if R ³ and R ⁴ together form a phenyl ring, wherein the at least one carboxylic acid is present in its protonated form or as carboxylate with a suitable counter ion.

According to a preferred embodiment of the composition,

R ¹ is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4- C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, C6-C20- alkylaryl, C6-C20-arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, C4-C20- heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl, wherein in case of more than one (hetero)aliphatic or (hetero)aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy; and R ² is selected from the group consisting of hydrogen atom, branched or unbranched C1-C5- alkyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1- C10-alkoxy, C5-C10-aryl, C6-C10-alkylaryl and C6-C10-arylalkyl, wherein in case of more than one aromatic ring system the ring systems are condensed or separate, wherein each residue R ² has at least one substituent R ^2a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy.

More preferably, the at least one carboxylic acid according to (b) is a carboxylic acid selected from the group consisting of diphenylacetic acid (DPAA), 2,2-diphenylpropionic acid (2DPPA), 3,3-diphenylpropionic acid (3DPPA), 3,4-dichloro-benzoic acid (34CA), 3,4-dinitro-benzoic acid (34NA) and 4-chloro-3-nitro-benzoic acid (43CNA), more preferably form the group consisting of diphenylacetic acid (DPAA), 2,2-diphenylpropionic acid (2DPPA) and 3,3-diphenylpropionic acid (3DPPA), more preferably 2,2-diphenylpropionic acid (2DPPA) or 3,3-diphenylpropionic acid (3DPPA), more preferably at least 3DPPA.

According to a further preferred embodiment of the composition, the residue R ¹ of the amine according to (a) is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4-C20- cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, C6-C20-alkylaryl, C6-C20- arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, C4-C20-heteroaryl, C5-C20- alkylheteroaryl and C5-C20-heteroarylalkyl, wherein the hetero atom(s) in C4-C20-heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl is/are oxgen or sulfur and the hetero atom(s) in C2-C20-heteroalkyl and C3-C20-cyclic heteroalkyl, is/are selected from oxygen, sulfur and nitrogen, wherein in case of more than one (hetero)aliphatic or (hetero)aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy. Preferably, the residue R ¹ of the amine according to (a) is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4-C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, C6- C20-alkylaryl, C6-C20-arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy. More preferably, the residue R ¹ of the amine according to (a) is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, C4-C20-cycloalkyl, C5- C20-cycloalkenyl, and C5-C20-cycloalkinyl, C5-C20-aryl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy. More preferably, the residue R ¹ of the amine according to (a) is selected from the group consisting of branched or unbranched C2- C10-alkyl, C5-C10-cycloalkyl and C5-C20-aryl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy; R ¹ being preferably selected from the group consisting of methyl, iso-propyl, cyclohexyl and phenyl, wherein phenyl has at least one substituent selected from the group consisting of hydrogen atom, halogen atom, preferably fluoro or chloro, and methoxy, preferably meta- or para-methoxy.

For R ¹ being branched or unbranched C2-C20-alkyl or branched or unbranched C2-C20- alkenyl, a preferred embodiment relates to R1 being branched or unbranched C4-C20-alkyl or branched or unbranched C4-C20-alkenyl.

According to a further preferred embodiment of the composition, the residue R ² of the amine according to (a) is selected from the group consisting of hydrogen atom, branched or unbranched C1-C5-alkyl, wherein each residue R ² has at least one substituent R ^2a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy. Preferably, the residue R ² of the amine according to (a) is selected from the group consisting of branched or unbranched C1-C3-alkyl, R ² being preferably methyl.

In a preferred embodiment of the composition, the combination of R ¹ , R ^1a being a perfluorinated alkyl is excluded. The same applies for R ² and R ^2a , i.e. the combination of R ² and R ^2a being a perfluorinated alkyl is excluded as well. In other words, neither the combination of R ¹ and R ^1a nor the combination of R ² and R ^2a is a perfluorinated alkyl.

Regarding the embodiment of the composition, wherein R ¹ and R ² together form a C3-C10- cycloalkyl or a C3-C10-cycloalkenyl, the number of C atoms indicated includes the carbonyl C atom situated between R ¹ and R ² .

According to a preferred embodiment of the composition, the composition comprises the amine according to (a) in an amount in the range of from 90 to 99.9 weight-%, preferably in an amount in the range of from 95 to 99.9 weight-%, more preferably in an amount in the range of from 98 to 99.9 weight-%. According to a further preferred embodiment of the composition, the composition comprises the at least one carboxylic acid according to (b) (protonated form or carboxylate with a suitable counter ion) in an amount of at least 0,003 weight-%, preferably in an amount in the range of from 0.003 to 5 weight-%, more preferably in an amount in the range of from 0.003 to 3 weight-%.

Below, the investigations carried out by the inventors are described in more detail:

As described above, commercially readily available aliphatic, aromatic and heteroaromatic carboxylic acids (R-COOH) were selected and screened as their respective carboxylate salts towards common amines from a transaminase-catalyzed reaction. 1-phenylethylamine and substituted derivatives 2a-f thereof served as model product amines and were compared with typical donor amines such as isopropylamine 3, racemic 2-butylamine, DL-alanine and L- alanine. The straight-forward screening approach especially resulted in the identification of two benzylbenzene-based acids and three benzoic acid derivatives that matched the required criteria: DPAA, 3DPPA, 34CA, 34NA and 43CNA. In addition, 2DPPA was identified as suitable carboxylic acid.

For example, the isopropylamine salt of 4-chloro-3-nitrobenzoic acid (43CNA) 5 shows a very high solubility of 993 mmol·l ^-1 , while the 1-phenylethylamine salt of 43CNA 6a is considerable less soluble with 22 mmol·l ^-1 . As stated by Le Chatelier’s principle, the solubility of amine salts can be further reduced if an over-stoichiometric amount of carboxylate is added to the mother liquor, which pushes the equilibrium from the dissociated forms (present in solution) towards its non-dissociated solid salt form.

Aside the general solubility difference, the applicability of these 3 acids - 43CNA, DPAA and 3DPPA - was tested with 7 exemplary amine transaminases from Aspergillus fumigates (AfAT A), Gibberella zeae (GzATA), Neosartorya fischeri (NfATA), Aspergillus oryzae (AoATA), Aspergillus terreus (AtATA), Mycobacterium vanbaalenii (MvAJA) and Silicibacter pomeroyi (SpATA) (Fig. 1 ). The results show that almost all investigated amine transaminases are already strongly inhibited by 50 mM of the more soluble acids 43CNA and DPAA. Herein MvATA and SpATA were identified as the most stable enzymes. A noticeable exception from these results is acid 3DPPA, which is only sparingly soluble in buffered solutions. This effectively limits the carboxylate concentration in aqueous solution to a maximum of≤25 mM, depending on temperature and pH, while the excess of solid 3DPPA remains in the reaction mixture. This low 3DPPA-concentration also does not significantly inhibit the investigated AT As. Fortunately, the investigated 3DPPA-salts exhibit the lowest solubility of product amine salt 6, which fits perfectly into the above mentioned ISPC-requirements (see Example section, Tables 4 and 5).

Consequently, 3DPPA was identified as the most valuable acid for the application in a crystallization-based in situ- product removal (ISPR) of amine 2 from an amine transaminase- catalyzed reaction.

The use of 3DPPA in combination with an exemplary SpATA-catalyzed conversion of 100 mM acetophenone 1a to (S)-l-phenylethylamine shows clearly the synthetic advantage of an acid- based ISPC (Fig. 2). The classical reaction approach with a low donor amine concentration of only 250 mM isopropylamine yields a non-sufficient conversion of 19%. A simple addition of 1.25 eq. solid 3DPPA improved the overall conversion directly to ca. 75%, regardless of the use as a whole cell biocatalyst or partially purified cell extract. The majority of product 2 is afterwards present as solid salt 6, which can be almost quantitatively recovered by filtration after cooling the reaction mixture to 0 °C. Consequently, this ISPC-concept with 3DPPA translates to a more atom-efficient synthesis since less donor amine is required and a simplified downstream processing-approach is facilitated (see below). Noteworthy, the low solubility of 3DPPA does not limit the crystallization of product amine salt since the constant removal of 3DPPA from aqueous solution is continuously compensated back to its original solubility limit by a

simultaneous dissolution of 3DPPA (from excess solid 3DPPA).

The shown ISPC-concept with acid 3DPPA was also successfully used for the SpATA-catalyzed conversion of selected acetophenone derivatives 1b-g and further non-aromatic substrates 1h-k (Table 2).

Table 2: ISPC-supported SpATA-catalyzed synthesis of chiral amines

As expected, for all substrates low conversions were obtained without ISPC due to the low, but still over-stochiometric, use of 250 mM isopropylamine. A simple addition of 3DPPA increases product formation significantly for almost all investigated substrates. Improvements range between 2 and 8.1 -fold with yields of up to 96 % for 1k, while the products are selectively crystallized as its 3DPPA-salts. The remaining mother liquor, including excess isopropylamine, can be directly reused for a further increase of atom efficiency of the transaminase-catalyzed reaction. Even higher donor amine concentrations will yield a further increase in conversion, but include the risk of an undesired crystallization of donor amine salt, which then eventually yields a decrease in product formation.

The isolation of product amine 2 is easily realized by dissolving product salt 6 in an aqueous solution at high pH, followed by an extraction and evaporation of the solvent, e.g. MTBE.

Alternatively, the respective hydrochloride salt can be directly crystallized from the ether phase by a careful addition of concentrated HCI. In addition, the spent acid 3DPPA can also be precipitated from the remaining aqueous phase by acidification with concentrated HCI, due to its low solubility at low pH.

Summarizing, the presented in situ-product crystallization of an amine from a transaminase- catalyzed reaction by the addition of a selected acid/carboxylate presents a powerful synthetic alternative to the use of tailor-made donor amines and complex cascade reaction systems. The main advantages of this ISPC are a more atom-efficient use of classical, cheap donor amines and a simplified downstream processing-approach by simple filtration. The targeted product amine can be afterwards extracted from its salt and the applied 3DPPA acid easily recycled.

The present invention is further illustrated by the following embodiments and combinations of embodiments as indicated by the respective dependencies and back-references. In particular, it is noted that in each instance where a range of embodiments is mentioned, for example in the context of a term such as "The process of any one of embodiments 1 to 4", every embodiment in this range is meant to be explicitly disclosed for the skilled person, i.e. the wording of this term is to be understood by the skilled person as being synonymous to "The process of any one of embodiments 1 , 2, 3, and 4".

1. Method for preparing an amino salt compound comprising:

i) providing a carbonyl compound of general formula (I)

wherein

R ¹ is selected from the group consisting of branched or unbranched C2-C20- alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4-C20-cycloalkyl, C5-C20- cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, C6-C20-alkylaryl, C6- C20-arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, C4-C20- heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl, wherein in case of more than one (hetero)aliphatic or (hetero)aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy; and

R ² is selected from the group consisting of hydrogen atom, branched or unbranched C1-C5-alkyl, branched or unbranched C1-C5-alkyl-O-C1-C5- alkyl, branched or unbranched C1-C10-alkoxy, C5-C10-aryl, C6-C10- alkylaryl and C6-C10-arylalkyl, wherein in case of more than one aromatic ring system the ring systems are condensed or separate, wherein each residue R ² has at least one substituent R ^2a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy;

or

R ¹ , R ² together form a C3-C10-cycloalkyl or C3-C10-cycloalkenyl, wherein the C3-C10-cycloalkyl or C3-C10-cycloalkenyl each has at least one substituent R ^x selected from the group consisting of hydrogen atom, C1- C5-alkyl, C1-C4-heteroalkyl and C1-C5-alkyl-R ^y , wherein R ^y is hydroxyl or thiol;

ii) reacting the carbonyl compound provided according to (i) in the presence of a transaminase with

ii-a) at least one primary amine; and

ii-b) at least one carboxylic acid;

thereby obtaining a mixture comprising an at least partially crystallized amino salt compound comprising

a cation of general formula (II)

wherein R ¹ and R ² are as defined for general formula (I) and a carboxylate anion based on the at least one carboxylic acid added

according to (ii-b). 2. The method according to embodiment 1 , wherein the amino salt compound obtained according to (ii) has a solubility in water at pH 7 which is smaller than the solubility in water of the at least one primary amine added according to (ii-a). 3. The method according to embodiment 1 or 2, wherein the amino salt compound

obtained according to (ii) has a solubility in water at pH 7≤ 30 mmol/l, preferably≤ 25 mmol/l, more preferably≤ 10 mmol/l. 4. The method according to any one of embodiments 1 to 3, wherein the residue R ¹ is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4- C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, C6-C20- alkylaryl, C6-C20-arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, C4-C20- heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl, wherein the hetero atom(s) in C4-C20-heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl is/are oxygen or sulfur and the hetero atom(s) in C2-C20-heteroalkyl andC3-C20-cyclic heteroalkyl, is/are selected from oxygen, sulfur and nitrogen, wherein in case of more than one (hetero)aliphatic or (hetero)aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy; 5. The method according to any one of embodiments 1 to 4, wherein the residue R ¹ is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4- C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, C6-C20- alkylaryl, C6-C20-arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, wherein the hetero atom(s) is/are selected from oxygen, sulfur and nitrogen wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy. 6. The method according to any one of embodiments 1 to 5, wherein the residue R ¹ is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, C4-C20- cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl and C5-C20-aryl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy.

7. The method according to any one of embodiments 1 to 6, wherein the residue R ¹ is selected from the group consisting of branched or unbranched C2-C10-alkyl, C5-C10- cycloalkyl and C5-C20-aryl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy; R ¹ being preferably selected from the group consisting of methyl, iso-propyl, cyclohexyl and phenyl, wherein phenyl has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom, preferably fluoro or chloro, and methoxy, preferably meta- or para-methoxy.

8. The method according to any one of embodiments 1 to 7, wherein the residue R ² is selected from the group consisting of hydrogen atom, branched or unbranched C1-C5- alkyl, wherein each residue R ² has at least one substituent R ^2a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy.

9. The method according to any one of embodiments 1 to 8, wherein the residue R ² is selected from the group of branched or unbranched C1-C3-alkyl, R ² being preferably methyl.

10. The method according to any one of embodiments 1 to 9, wherein the transaminase according to (ii) is selected from the group of transaminases, preferably from the group of amine transaminases, , more preferably selected from the group consisting of amine transaminase from Aspergillus fumigates (AfATA) according to SEQ ID NO 1 , amine transaminase from Gibberella zeae (GzATA) according to SEQ ID NO 2, amine transaminase from Neosartorya fischeri (NfATA) according to SEQ ID NO 3, amine transaminase from Aspergillus oryzae (AoATA) according to SEQ ID NO 4, amine transaminase from Aspergillus terreus (AtATA) according to SEQ ID NO 5, amine transaminase from Mycobacterium vanbaalenii (MvATA) according to SEQ ID NO 6, amine transaminase from Silicibacter pomeroyi (SpATA) according to SEQ ID NO 7 and a homologue enzyme having sequence identity of at least 65% with any one of SEQ ID NO 1 to 7 and having the same function as the amine transaminase of SEQ ID NO 1 to 7, more preferably selected from the group consisting of the amine transaminase from Mycobacterium vanbaalenii (MvATA) according to SEQ ID NO 6, the amine

transaminase from Silicibacter pomeroyi (SpATA) according to SEQ ID NO 7 and a homologue enzyme having sequence identity of at least 65% with any one of SEQ ID NO 6 or 7 and having the same function as the amine transaminase of SEQ ID NO 6 or 7. 11. The method according to embodiment 10, wherein the homologue enzyme has a sequence identity of at least 75%, preferably at least 85%, more preferably at least 90%, more preferably at least 95%, more preferably at least 98%, more preferably at least 99%, with any one of SEQ ID NO 1 to 7 and has the same function as the amine transaminase of SEQ ID NO 1 to 7. 12. The method according to any one of embodiments 1 to 11 , wherein the at least one primary amine according to (ii-a) is used in non-protonated form or in protonated form with a suitable counter anion. 13. The method according to any one of embodiments 1 to 12, wherein the at least one primary amine according to (ii-a) is selected from the group of mono- and diamines having one to 10 carbon atoms, preferably from the group consisting of 1 ,5-diamino- pentane (cadaverine), alanine, 2-amino-butane (sec-butylamine) and 2-amino-propane, and is preferably 2-amino-propane (iso-propylamine) in its non-protonated or protonated form, wherein the protonated form is present in combination with a suitable anion. 14. The method according to any one of embodiments 1 to 13, wherein the at least one carboxylic acid according to (ii-b) is used in its protonated form or in deprotonated form with a suitable counter cation. 13. The method according to any one of embodiments 1 to 12, wherein the at least one carboxylic acid according to (ii-b) is a carboxylic acid of general formula (III)

wherein n is zero or 1 ;

the residues R ³ and R ⁴ are both phenyl or together form a phenyl ring, wherein each phenyl ring has at least one further substituent selected from the group consisting of hydrogen atom, halogen atom, preferably chloro, and nitro group; and the residue R ⁵ is hydrogen atom or methyl or absent if R ³ and R ⁴ together form a phenyl ring; preferably the at least one carboxylic acid according to (ii-b) is a carboxylic acid selected from the group consisting of diphenylacetic acid (DPAA), 2,2-diphenylpropionic acid (2DPPA), 3,3-diphenylpropionic acid (3DPPA), 3,4-dichloro-benzoic acid (34CA), 3,4-dinitro- benzoic acid (34NA) and 4-chloro-3-nitro-benzoic acid (43CNA), more preferably from the group consisting of diphenylacetic acid (DPAA), 2,2-diphenylpropionic acid (2DPPA) and 3,3-diphenylpropionic acid (3DPPA), more preferably 2,2-diphenylpropionic acid (2DPPA) or 3,3-diphenylpropionic acid (3DPPA), more preferably at least 3DPPA. 16. The method according to any one of embodiments 1 to 15, wherein the at least one primary amine according to (ii-a) and the at least one carboxylic acid according to (ii-b) are used as one or more salt(s) comprising the protonated form of the at least one primary amine and the deprotonated form of the at least one carboxylic acid, preferably as one salt comprising the protonated form of the at least one primary amine and the deprotonated form of the at least one carboxylic acid, more preferably as isopropyl ammonium 3,3-diphenylpropionate.

17. The method according to any one of embodiments 1 to 16, wherein the amino salt compound obtained according to (ii) comprises a cation of general formula (II)

wherein R ¹ and R ² are as defined for general formula (I), and an anion based on the at least one carboxylic acid, which is preferably an anion of general formula (Ilia)

wherein n is zero or 1 ;

the residues R ³ and R ⁴ are both phenyl or together form a phenyl ring, wherein each phenyl ring has at least one further substituent selected from the group consisting of hydrogen atom, halogen atom, preferably chloro, and nitro group and the residue R ⁵ is hydrogen atom or methyl or absent if R ³ and R ⁴ together form a phenyl ring; wherein the anion of general formula (Ilia) is preferably selected from the group consisting of diphenylacetate, 2,2-diphenylpropionat, 3,3-diphenylpropioniat, 3,4-dichloro-benzoat, 3,4-dinitro-benzoat and 4-chloro-3-nitro-benzoat, more preferably form the group consisting of diphenylacetate, 2,2-diphenylpropionat, 3,3-diphenylpropioniat, more preferably 2,2-diphenylpropionat or 3,3-diphenylpropioniat, more preferably 3,3- diphenylpropioniat.

18. The method according any one of embodiments 1 to 17, wherein the reaction according to (ii) is carried out in an aqueous solution, which preferably comprises at least 80 weight-%, more preferably at least 90 weight-%, more preferably at least 95 weight-%, more preferably at least 98 weight-%, water, based on the overall weight of the aqueous solution.

19. The method according to embodiment 18, wherein the aqueous solution comprises a buffer, preferably selected from the group of tris(hydroxymethyl)aminomethane buffer (TRIS buffer), 3-(N-morpholino)propanesulfonic acid buffer (MOPS buffer), N,N-Bis(2- hydroxyethyl)-2-aminoethanesulfonic acid buffer (BES buffer), N- (tris(hydroxymethyl)methyl)glycine buffer (Tricine buffer), Carbonate buffer, N- cyclohexyl-2-aminoethanesulfonic acid buffer (CHES buffer), 4-(2-hydroxyethyl)-1- piperazineethanesulfonic acid buffer (HEPES buffer) and phosphate buffer, more preferably at least a phosphate buffer. 20. The method according to any one of embodiments 1 to 19, wherein the reaction

according to (ii) is carried out at a pH value in the range of 6.0 to 9.5, preferably in the range of from 6.5 to 9.0, more preferably in the range of from 7.0 to 8.0. 21. The method according to any one of embodiments 1 to 20, wherein the reaction

according to (ii) is carried out for a time period of at least one hour, preferably for a time in the range of from 1 to 1 ,000 hours, more preferably in the range of from 5 to 500 hours, more preferably in the range of from 10 to 200 hours. 22. The method according to any one of embodiments 1 to 21 , wherein the reaction

according to (ii) is carried out at a temperature in the range of from 10 to 50 °C, preferably in the range of from 15 to 45 °C, more preferably in the range of from 20 to 40 °C, more preferably in the range of from 25 to 35 °C. 23. The method according to any one of embodiments 1 to 22, wherein for the at least one carboxylic acid being a carboxylic acid according to general formula (III), wherein the residues R ³ and R ⁴ together form a phenyl ring, preferably a carboxylic acid selected from the group consisting of 3,4-dichloro-benzoic acid (34CA), 3,4-dinitro-benzoic acid (34NA) and 4-chloro-3-nitro-benzoic acid (43CNA), the concentration of the at least one carboxylic acid is kept in the range of from 0.001 to 50 mM, preferably in the range of form 1 to 45 mM, more preferably in the range of from 5 to 40 mM during step (ii). 24. The method according to any one of embodiments 1 to 22, wherein for the at least one carboxylic acid being a carboxylic acid according to general formula (III), wherein the residues R ³ and R ⁴ are each a phenyl ring, preferably a carboxylic acid selected from the group consisting of diphenylacetic acid (DPAA), 2,2-diphenylpropionic acid (2DPPA) and 3,3-diphenylpropionic acid (3DPPA), the concentration of the at least one carboxylic acid is≤50 mM during step (ii). 25. The method according to any one of embodiments 1 to 24, further comprising:

iii) separating the at least partially crystallized amine salt compound obtained

according to (ii) from the mixture thereby obtaining the crystallized amine salt compound. 26. The method according to embodiment 26, wherein separating the crystallized amine salt compound according to (iii) from the mixture is done by sedimentation, centrifugation or filtration, preferably by filtration. 27. The method according to any one of embodiments 1 to 24, further comprising: (iv) optionally washing the separated crystallized amino salt compound obtained according to (iii), preferably with water or an organic solvent or a mixture thereof, more preferably with water or methyl tert-butyl ether or a mixture thereof, thereby obtaining a washed crystallized amino salt compound;

(v) dissolving the crystallized amino salt compound obtained according to (iii) or optionally the washed crystallized amino salt compound obtained according to (iv) in an aqueous solution having a pH value in the range of from 10 to 14 comprising at least one base, preferably a base comprising a hydroxide ion, thereby obtaining an aqueous solution comprising an amine of general formula (I la)

wherein R ¹ and R ² are as defined for general formula (I);

(vi) extracting the aqueous solution obtained according to (v) at least once with a water immiscible organic solvent obtaining an organic phase comprising at least parts of the amine of general formula (I la);

and an aqueous phase comprising at least parts of the anion of general formula (Ilia)

wherein n is zero or 1 ; and wherein the residues R ³ and R ⁴ are both phenyl or together form a phenyl ring, wherein each phenyl ring has at least one further substituent selected from the group consisting of hydrogen atom, halogen atom, preferably chloro, and nitro group and the residue R ⁵ is hydrogen atom or methyl or absent if R ³ and R ⁴ together form a phenyl ring; wherein the anion of general formula (Ilia) is preferably selected from the group consisting of diphenylacetate, 2,2-diphenylpropionat, 3,3-diphenylpropioniat, 3,4-dichloro-benzoat, 3,4-dinitro- benzoat and 4-chloro-3-nitro-benzoat, more preferably from the group consisting of diphenylacetate, 2,2-diphenylpropionat, 3,3-diphenylpropioniat, more preferably 2,2-diphenylpropionat or 3,3-diphenylpropioniat, more preferably 3,3- diphenylpropioniat. 28. The method according to embodiment 27, further comprising:

(vii-a) removal of the water immiscible organic solvent from the organic phase obtained in (vi) thereby obtaining the amine of general formula (I la),

wherein R ¹ and R ² are as defined for general formula (I). 29. The method according to embodiment 27 further comprising:

(vii-b) adding at least one acid HX to the organic phase obtained according to (vi), preferably HCI, thereby obtaining a salt of general formula (IV)

wherein R ¹ and R ² are as defined for general formula (I) and (II) and X is an ion based on the at least one acid HX, preferably Cl. 30. The method according to embodiment 27 or 28, wherein the water immiscible organic solvent according to (vi) has a Kow value of at least 0.5, more preferably of at least 0.6, more preferably of at least 0.7, more preferably of at least 0.8. 31. The method according to any one of embodiments 27 to 30, further comprising:

(viii) optionally precipitating the at least one carboxylic acid of general formula (III)

wherein n is zero or 1 ;

the residues R ³ and R ⁴ are both phenyl or together form a phenyl ring, wherein each phenyl ring has at least one further substituent selected from the group consisting of hydrogen atom, halogen atom, preferably chloro, and nitro group and the residue R ⁵ is hydrogen atom or methyl or absent if R ³ and R ⁴ together form a phenyl ring; preferably the at least one carboxylic acid being selected from the group consisting of diphenylacetic acid (DPAA), 2,2-diphenylpropionic acid (2DPPA), 3,3-diphenylpropionic acid (3DPPA), 3,4-dichloro-benzoic acid (34CA), 3,4-dinitro-benzoic acid (34NA) and 4-chloro-3-nitro-benzoic acid (43CNA), more preferably form the group consisting of diphenylacetic acid (DPAA), 2,2- diphenylpropionic acid (2DPPA) and 3,3-diphenylpropionic acid (3DPPA), more preferably 2,2-diphenylpropionic acid (2DPPA) or 3,3-diphenylpropionic acid (3DPPA), more preferably at least 3DPPA,

from the aqueous phase obtained according to (vi) by adjusting the pH to a value in the range of from 0 to 6, preferably by addition of HCI, and

(ix) optionally recycling the at least one carboxylic acid precipitated according to (viii) to the process, preferably to step (ii). 32. An amino salt compound obtained or obtainable by the method according to any one of embodiments 1 to 31. 33. An amino salt compound comprising a cation of general formula (II)

wherein

R ¹ is selected from the group consisting of branched or unbranched C2-C20- alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4-C20-cycloalkyl, C5-C20- cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, C6-C20-alkylaryl, C6- C20-arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, C4-C20- heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl, wherein in case of more than one (hetero)aliphatic or (hetero)aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy; and

R ² is selected from the group consisting of hydrogen atom, branched or unbranched C1-C5-alkyl, branched or unbranched C1-C5-alkyl-O-C1-C5- alkyl, branched or unbranched C1-C10-alkoxy, C5-C10-aryl, C6-C10- alkylaryl and C6-C10-arylalkyl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ² has at least one substituent R ^2a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3- alkoxy; or

R ¹ , R ² together form a C3-C10-cycloalkyl or C3-C10-cycloalkenyl, wherein the C3-C10-cycloalkyl or C3-C10-cycloalkenyl each has at least one substituent R ^x selected from the group consisting of hydrogen atom, C1- C5-alkyl, C1-C4-heteroalkyl and C1-C5-alkyl-R ^y , wherein R ^y is hydroxyl or thiol;

and

an anion of general formula (Ilia)

wherein n is zero or 1 ;

the residues R ³ and R ⁴ are both phenyl or together form a phenyl ring, wherein each phenyl ring has at least one further substituent selected from the group consisting of hydrogen atom, halogen atom, preferably chloro, and nitro group and the residue R ⁵ is hydrogen atom or methyl or absent if R ³ and R ⁴ together form a phenyl ring. 34. The amino salt compound according to embodiment 33, wherein the anion of general formula (Ilia) is preferably selected from the group consisting of diphenylacetate, 2,2- diphenylpropionate, 3,3-diphenylpropionate, 3,4-dichloro-benzoate, 3,4-dinitro-benzoate and 4-chloro-3-nitro-benzoate, more preferably from the group consisting of

diphenylacetate, 2,2-diphenylpropionate, 3,3-diphenylpropionate, more preferably 2,2- diphenylpropionate or 3,3-diphenylpropionate, more preferably 3,3-diphenylpropionate. 35. The amino salt compound according to embodiment 33 or 34, wherein the residue R ¹ is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4- C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, C6-C20- alkylaryl, C6-C20-arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, C4-C20- heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl, wherein the hetero atom(s) in C4-C20-heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl is/are oxgen or sulfur and the hetero atom(s) in C2-C20-heteroalkyl and C3-C20-cyclic heteroalkyl, is/are selected from oxygen, sulfur and nitrogen, wherein in case of more than one (hetero)aliphatic or (hetero)aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy; 36. The amino salt compound according to any one of embodiments 33 to 35, wherein the residue R ¹ is selected from the group consisting of branched or unbranched C2-C20- alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10- alkoxy, C4-C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, C6- C20-alkylaryl, C6-C20-arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy. 37. The amino salt compound according to any one of embodiments 33 to 36, wherein the residue R ¹ is selected from the group consisting of branched or unbranched C2-C20- alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, C4-C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy.

38. The amino salt compound according to any one of embodiments 33 to 37, wherein the residue R ¹ is selected from the group consisting of branched or unbranched C2-C10- alkyl, C5-C10-cycloalkyl and C5-C20-aryl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy; R ¹ being preferably selected from the group consisting of methyl, iso-propyl, cyclohexyl and phenyl, wherein phenyl has at least one substituent selected from the group consisting of hydrogen atom, halogen atom, preferably fluoro or chloro, and methoxy, preferably meta- or para-methoxy.

39. The amino salt compound according to any one of embodiments 33 to 38, wherein the residue R ² is selected from the group consisting of hydrogen atom, branched or unbranched C1-C5-alkyl, wherein each residue R ² has at least one substituent R ^2a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy.

40. The amino salt compound according to any one of embodiments 33 to 39, wherein the residue R ² is selected from the group consisting of branched or unbranched C1-C3-alkyl, R ² being preferably methyl.

41. A composition comprising

a) an amine of general formula (I la)

wherein

R ¹ is selected from the group consisting of branched or unbranched C2-C20- alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4-C20-cycloalkyl, C5-C20- cycloalkenyl, C5-C20-cycloalkinyl, C5-C20-aryl, C6-C20-alkylaryl, C6- C20-arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, C4-C20- heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl, wherein in case of more than one (hetero)aliphatic or (hetero)aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy; and R ² is selected from the group consisting of hydrogen atom, branched or unbranched C1-C5-alkyl, branched or unbranched C1-C5-alkyl-O-C1-C5- alkyl, branched or unbranched C1-C10-alkoxy, C5-C10-aryl, C6-C10- alkylaryl and C6-C10-arylalkyl, wherein in case of more than one aromatic ring system the ring systems are condensed or separate, wherein each residue R ² has at least one substituent R ^2a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy; or R ¹ , R ² together form a C3-C10-cycloalkyl or C3-C10-cycloalkenyl, wherein the C3-C10-cycloalkyl or C3-C10-cycloalkenyl each has at least one substituent R ^x selected from the group consisting of hydrogen atom, C1- C5-alkyl, C1-C4-heteroalkyl and C1-C5-alkyl-R ^y , wherein R ^y is hydroxyl or thiol;

and

b) at least one carboxylic acid of general formula (III)

wherein n is zero or 1 ;

the residues R ³ and R ⁴ are both phenyl or together form a phenyl ring, wherein each phenyl ring has at least one further substituent selected from the group consisting of hydrogen atom, halogen atom, preferably chloro, and nitro group; and the residue R ⁵ is hydrogen atom or methyl or absent if R ³ and R ⁴ together form a phenyl ring, wherein the at least one carboxylic acid is present in its protonated form or as carboxylate with a suitable counter ion.

42. The composition according to embodiment 41 , wherein the at least one carboxylic acid according to (b) is a carboxylic acid selected from the group consisting of diphenylacetic acid (DPAA), 2,2-diphenylpropionic acid (2DPPA), 3,3-diphenylpropionic acid (3DPPA), 3,4-dichloro-benzoic acid (34CA), 3,4-dinitro-benzoic acid (34NA) and 4-chloro-3-nitro- benzoic acid (43CNA), more preferably form the group consisting of diphenylacetic acid (DPAA), 2,2-diphenylpropionic acid (2DPPA) and 3,3-diphenylpropionic acid (3DPPA), more preferably 2,2-diphenylpropionic acid (2DPPA) or 3,3-diphenylpropionic acid (3DPPA), more preferably at least 3DPPA.

43. The composition according to embodiment 41 or 42, wherein the residue R ¹ of the amine according to (a) is selected from the group consisting of branched or unbranched C2- C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20- alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4-C20-cycloalkyl, C5-C20-cycloalkenyl, C5-C20-cycloalkinyl, C5-C20- aryl, C6-C20-alkylaryl, C6-C20-arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, C4-C20-heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl, wherein the hetero atom(s) in C4-C20-heteroaryl, C5-C20-alkylheteroaryl and C5-C20-heteroarylalkyl is/are oxgen or sulfur and the hetero atom(s) in C2-C20-heteroalkyl and C3-C20-cyclic heteroalkyl, is/are selected from oxygen, sulfur and nitrogen, wherein in case of more than one (hetero)aliphatic or (hetero)aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1-C3-alkoxy.

44. The composition according to any one of embodiments 41 to 43, wherein the residue R ¹ of the amine according to (a) is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, branched or unbranched C1-C5-alkyl-O-C1-C5-alkyl, branched or unbranched C1-C10-alkoxy, C4-C20-cycloalkyl, C5-C20-cycloalkenyl, C5- C20-cycloalkinyl, C5-C20-aryl, C6-C20-alkylaryl, C6-C20-arylalkyl, C2-C20-heteroalkyl, C3-C20-cyclic heteroalkyl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom (F, Cl, Br, I), hydroxyl, thiol, C1-C3 thioester, C1-C3-thioether, C1-C3-alkyl and C1- C3-alkoxy.

45. The composition according to any one of embodiments 41 to 44, wherein the residue R ¹ of the amine according to (a) is selected from the group consisting of branched or unbranched C2-C20-alkyl, branched or unbranched C2-C20-alkenyl, branched or unbranched C2-C20-alkinyl, C4-C20-cycloalkyl, C5-C20-cycloalkenyl, and C5-C20- cycloalkinyl, C5-C20-aryl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy.

46. The composition according to any one of embodiments 41 to 45, wherein the residue R ¹ of the amine according to (a) is selected from the group consisting of branched or unbranched C2-C10-alkyl, C5-C 10-cycloalkyl and C5-C20-aryl, wherein in case of more than one aliphatic or aromatic ring system the ring systems are condensed or separate, wherein each residue R ¹ has at least one substituent R ^1a selected from the group consisting of hydrogen atom, halogen atom, C1-C3-alkyl and C1-C3-alkoxy; R ¹ being preferably selected from the group consisting of methyl, iso-propyl, cyclohexyl and phenyl, wherein phenyl has at least one substituent selected from the group consisting of hydrogen atom, halogen atom, preferably fluoro or chloro, and methoxy, preferably meta- or para-methoxy.

47. The composition according to any one of embodiments 41 to 46, wherein the residue R ² of the amine according to (a) is selected from the group consisting of hydrogen atom, branched or unbranched C1-C5-alkyl, wherein each residue R ² has at least one substituent R ^2a selected from the group consisting of hydrogen atom, halogen atom, C1- C3-alkyl and C1-C3-alkoxy.

48. The composition according to any one of embodiments 41 to 47, wherein the residue R ² of the amine according to (a) is selected from the group consisting of branched or unbranched C1-C3-alkyl, R ² being preferably methyl.

49. The composition according to any one of embodiments 41 to 48, wherein the

composition comprises the amine according to (a) in an amount in the range of from 90 to 99.9 weight-%, preferably in an amount in the range of from 95 to 99.9 weight-%, more preferably in an amount in the range of from 98 to 99.9 weight-%.

50. The composition according to any one of embodiments 41 to 49, wherein the

composition comprises the at least one carboxylic acid according to (b) (protonated form or carboxylate with a suitable counter ion) in an amount of at least 0,003 weight-%, preferably in an amount in the range of from 0,003 to 5 weight-%, more preferably in an amount in the range of from 0,003 to 3 weight-%.

Description of Figures

Fig. 1 Effects of 43CNA, DPAA and 3DPPA on selected amine transaminases;

Conditions: 200 mM phosphate buffer pH 7.5, 10 mM acetophenone 1 , 500 mM (43CNA and DPAA) or 250 mM (3DDPA) isopropylamine, 5 mg-mL ^-1 lyophilized cell extract, 30 °C, 22 h; the obtained concentrations of 2 were intentionally held below the solubility limit of product salt 6 to prevent an undesired in situ-product crystallization; 43CNA was chosen as a representative of the identified benzoic acid derivatives;

Fig. 2 Time progression curves for the SpTA-catalyzed formation of (S)-l-phenylethyl- amine with and without in situ-product crystallization (ISPC); Ill-whole cells or ■-cell extract with 125 mM 3DPPA, O-whole cells or●-0611 extract without 3DPPA; Conditions: 200 mM phosphate buffer pH 7.5, 100 mM acetophenone, 250 mM isopropylamine, 15 mg-mL· ¹ lyophilized cell extract or whole cells, 30 °C;

Fig. 3: Exemplary result for the precipitation of (S)-4-Chloro-1-phenylethylamine salts.

Experimental Section

1. General information

Materials: All chemicals were obtained from commercial suppliers and used as received.

Deionized water was used throughout this study. The investigated enzymes (raw extract and whole cells) were received from Enzymicals AG (Greifswald, Germany) as lyophilizates; ECS- ATA01 (TA from Aspergillus fumigates, SEQ ID NO. 1), ECS-ATA02 (TA from Gibberella zeae, SEQ ID NO.2), ECS-ATA03 (TA from Neosartorya fischeri, SEQ ID NO.3), ECS-ATA04 (TA from Aspergillus oryzae, SEQ ID NO. 4), ECS-ATA05 (TA from Aspergillus terreus, SEQ ID NO. 5), ECS-ATA07 (TA from Mycobacterium vanbaalenii, SEQ ID NO. 6) and ECS-ATA08 (TA from Silicibacter pomeroyi, SEQ ID NO. 7).

Gas chromatography: Conversion was measured with a Trace 1310 gaschromatograph by Thermo Scientific (Dreieich, Germany), equipped with a 1300 flame ionization detector and a Chirasil-Dex-CB-column (25 m x 0.25 mm x 0.25 pm). n-Decane was used as internal standard in all measurements. Temperatures of injector and detector were set to 250 °C.

Temperature programs:

Compounds 1 a/2a, 1 b/2b and 1 c/2c: start at 90 °C, followed by a heating rate of 2 K/min to 1 14 °C and 20 K/min to 150 °C

Compounds 1 d/2d, 1 e/2e, 1f/2f and 1 g/2g: Start at 90 °C, followed by a heating rate of 2 K/min to 100 °C, 20 K/min to 130 °C, 2 K/min to 150 °C and 20 K/min to 160 °C

Compounds 1 i/2i, 1 j/2j , 1 k/2k: Start at 90 °C, followed by a heating rate of 2 K/min to 96 °C and 20 K/min to 1 10 °C.

HPLC: Enantiomeric excess was measured with a 1 100 Series HPLC by Agilent (Santa Clara, California, United States), equipped with a diode array detector, with a Chiralcel OD-H (250 mm length, 4.6 mm internal diameter, particle size: 5 pm) and a flow of 1 mL/min at 25 °C. Eluent composition for the respective amine: 99% n-heptane/ 1 % ethanol for 2f; 98% n-heptane/ 2% ethanol for 2b, 2c and 2g; 95% n-heptane/ 5% ethanol for 2a, 2d and2e

Enzyme Activity Assay: Enzyme activity was measured at a wave length of 245 nM with the spectrophotometer Specord 200 from Analytik Jena (Jena, Germany). Extinction coefficient of acetophenone: 1 1.852 (mM*cm)- ¹ .

Composition of the assay: 250 μL buffer solution, 250 μL 10 mM (S)-l-phenylethylamine in buffer solution, 250 μL 10 mM sodium pyruvate in buffer solution and 250 μL enzyme sample in buffer solution with 0.1 mM pyridoxal phosphate. All measurements were measured against a reference solution, whereas the enzyme solution was replaced with 200 μL buffer solution and 50 μL of 10 mM pyridoxal phosphate in buffer solution. Buffer solution: 50 mM phosphate buffer pH 8 with 0.25% DMSO.

2. Investigated acids for the in situ-product crystallization of amines

A total of 79 acids were chosen for the screening procedure of relevant amines (table 3). The selection is mostly based on commercial availability and stability in aqueous solution. Table 3: List of investigated acids for the ISPC-concept

3. Precipitation screening for suitable a ds

Screening of suitable acids was conducted with enantiomerically pure 1-phenylethylamine 2a and 6 derivatives thereof as model product amines at 50 mM. As typical donor amines racemic 2-butylamine, racemic alanine & L-alanine (at 100 mM) and isopropylamine 3 & racemic 1- phenylethylamine rac-2a (at 250 mM & 1000 mM) were chosen (scheme 3). The choice of the respective product amine enantiomer is not relevant for solubility screening since enantiomers have identical physical-chemical properties (incl. solubility), except its rotation of plane-polarized light in opposite directions. Results with racemic amines may differ significantly.

Scheme 3: Exemplary product and donor amines for acid screening Neutralized acid solutions:

All 79 separate 400 mM acid solutions (typically 20 ml.) were prepared by dissolving the respective acid in 50 mM phosphate buffer pH 7.5. Afterwards within all resulting solutions the pH was carefully adjusted back to 7.5. Please note that acids with low aqueous solubility may require multiple pH adjustments due to an additional dissolution process after its previous pH- adjustment. Acid solution with a remaining solid fraction were filtered and used in their resulting (unknown) concentration.

Neutralized amine solutions:

The selected exemplary product amines were dissolved in 50 mM phosphate buffer pH 7.5 with a concentration of 100 mM each and the pH carefully adjusted back to 7.5. Similarly solutions of the donor amines were prepared (200 mM for racemic 2 butylamine, racemic alanine and L- alanine and 500 mM & 2000 mM for isopropylamine and racemic 1-phenylethylamine). Precipitation screening procedure

200 μi fractions of the neutralized acid solutions (79 in total) were given each into a 96 well plate and their position documented. Afterwards 200 μi of one neutralized amine solution was added into each filled well, which led to a clear solution or an almost instantaneous precipitation. The result was documented by visual observation and photography against a black background after 1 and 24 h. Fig. 3 shows an exemplary result for (S)-4-Chloro-1-phenylethylamine salts after 1 hour. The procedure was repeated for all amine solutions and the results compared against each other (table 4). The intensity of precipitation, as shown by shade code, serves as a qualitative approximation of salt solubilities and their differences.

Table 4: graphical presentation of the screening results

description of symbols and grey

shade code for Table 3

The results of table 3 show clearly that certain acids allow significant differences in solubility between investigated salts. In this screening especially differences between product amines and the commonly used donor amines isopropylamine/alanine were targeted. Based on this consideration the following acids appear most applicable: 34CA, 34NA, 43CNA and 3DPPA. In addition, 2DPPA was identified as suitable acid. Acids with less strong differences are PCPA, 24CNA, 25CNA, 35DNOT, 3NA and 435CNBA, which might be useful for other product amines. PCPA was later excluded from the list of potential acids due to an unknown decomposition reaction of certain salt solutions (strong discoloration).

4. transaminase-catalyzed synthesis of product amines in combination with an in situ- product crystallization

General semi-preparative procedure for the amine transaminase-catalyzed synthesis of 2a-k in combination with an in situ-product crystallization of the product amine 6a-k via 3DPPA: To 25 ml 200 mM phosphate buffer pH 7.5 532 μL isopropylamine (= 250 mM) and 707 mg 3DPPA 125 mM) were given and the resulting suspension adjusted to pH 7.5 with aqueous H ₃ PO ₄ - solution. Afterwards PLP, substrate (= 100 mM) and biocatalyst were added and the resulting mixture shaken at 200 rpm. After completion of the reaction the resulting mixture was filtered to obtain the formed product amine salt. (This solid will contain remaining biocatalyst and excess 3DPPA.) Afterwards the solid fraction was washed with 10 ml. MTBE to remove remaining substrate and parts of excess 3DPPA. The solid was then given into 5 ml. water, 0,5 ml cone. NaOH was added to increase pH and formed product 2 extracted with 5 ml. MTBE. After phase separation the product was obtained as its hydrochloride by a slow addition of cone. HCI to the ether phase. 3DPPA can be precipitated from the remaining aqueous solution by adding cone. HCI, e.g. for recycling (isolated yield 71 %).

General reaction control procedure: Samples (500 μL) were taken periodically and thoroughly mixed by a vortex mixer with 50 μi cone. NaOH to quench the reaction and increase pH.

Afterwards 500 μL MTBE were added, mixed again by a vortex mixer and centrifuged (2 min, 3000 rpm) to improve phase separation. 200 μi were taken from the organic layer, combined with 50 μi of a 25 mM n-decane-solution in MTBE (internal standard) and subsequently analyzed by gas chromatography (column: CP-Chirasil-Dex CB; 25 m, 0.25 mm, 0.25 pm by Agilent, USA)