METHODS OF MAKING ORGANIC COMPOUNDS BY METATHESIS

CROSS-REFERENCE TO RELATED APPLICATIONS This application claims the benefit of U.S. Provisional Application having

Serial Number 60/851 ,632, filed October 13, 2006, and entitled METHODS OF MAKING ORGANIC COMPOUNDS BY METATHESIS, the disclosure of which is incorporated herein by reference.

GOVERNMENT RIGHTS This invention was made with U.S. Government support under Award

Number DE-FG36-04GO14016 awarded by the U.S. Department of Energy. The Government may have certain rights in this invention.

BACKGROUND It is desirable to use renewable feedstocks (e.g., natural oil-derived fatty acids or fatty esters) as a source material for synthesizing industrially important organic compounds that have been conventionally manufactured from petroleum feedstocks. One useful reaction for modifying the structure of natural oil-derived feedstocks is metathesis. Metathesis is a catalytic reaction involving the rupture and reformation of carbon-carbon double bonds. When metathesis is applied directly to many natural oil-derived feedstocks, a mixture of products results. For example, when metathesis is applied to a mixture of fatty acid esters, the resulting metathesis products include a mixture of monoesters and diesters of various chain lengths. Due to the similarity in molecular weight and functionality of the products, it is difficult to separate the desired product (e.g., a particular chain length diester) from the other metathesis products.

In view of the foregoing, what is desired is a method by which bifunctional compounds such as dicarboxylic acids, dicarboxylate esters, and dicarboxylate salt compounds can be manufactured in high yields from metathesis reactions applied to starting materials such as fatty acids, fatty esters, fatty acid salts, and mixtures thereof.

SUMMARY

The invention relates to methods of making organic compounds by metathesis chemistry. The methods of the invention are particularly useful for making industrially-important organic compounds from starting compositions that are derived from renewable feedstocks, such as natural oils.

The methods of the invention make use of a cross-metathesis step with an olefin compound to produce functionalized alkene intermediates having a predetermined double bond position. Advantageously, the functionalized alkene intermediates can be isolated at high purity from the other cross-metathesis products and from any remaining starting material. Once isolated, the functionalized alkene intermediate can be self-metathesized or cross-metathesized (e.g., with a second functionalized alkene) to produce the desired bifunctional organic compound or a precursor thereto. Representative organic compounds include bifunctional organic compounds, such as diacids, diesters, dicarboxylate salts, acid/esters, acid/amines, acid/alcohols, acid/aldehydes, acid/ketones, acid/halides, acid/nitriles, ester/amines, ester/alcohols, ester/aldehydes, ester/ketones, ester/halides, ester/nitriles, and the like.

Accordingly, in one aspect, the invention provides a method of making diacid alkenes, diester alkenes, or dicarboxylate salt alkenes by metathesis. The method of the invention comprises the steps of:

(a) providing a starting composition comprising one or more unsaturated fatty acids, unsaturated fatty esters, or unsaturated fatty acid salts;

(b) cross-metathesizing the composition of step (a) with a short-chain olefin in the presence of a first metathesis catalyst, to form cross-metathesis products comprising: (i) one or more olefins; and (ii) one or more acid-, ester-, or carboxylate salt-functionalized alkenes;

(c) separating at least a portion of one or more of the acid-, ester-, or carboxylate salt-functionalized alkenes from the cross-metathesis products; and

(d) self-metathesizing the separated acid-, ester-, or carboxylate salt- functionalized alkene in the presence of a second metathesis catalyst to form a composition comprising one or more diacid alkenes, diester alkenes, or dicarboxylate salt alkenes.

In another aspect, the invention provides a method of making bifunctional organic compounds, the method comprising the steps of:

(a) providing a starting composition comprising one or more unsaturated fatty acids, unsaturated fatty esters, or unsaturated fatty acid salts;

(b) cross-metathesizing the starting composition of step (a) with a short-chain olefin in the presence of a first metathesis catalyst to form cross- metathesis products comprising: (i) one or more olefins; and (ii) one or more acid-, ester-, or carboxylate salt-functionalized alkenes; (c) separating at least a portion of the one or more acid-, ester-, or carboxylate salt-functionalized alkenes from the cross-metathesis products; and

(d) cross-metathesizing the separated acid-, ester-, or carboxylate salt-functionalized alkenes with a second functionalized alkene in the presence of a metathesis catalyst to form a composition comprising a bifunctional organic compound.

BRIEF DESCRIPTION OF THE DRAWINGS FlG. 1 is a process flow diagram of an embodiment of the method of the invention. FlG. 2 is a process flow diagram of an embodiment of the method of the invention.

FIG. 2A is a process flow diagram of an embodiment of the method of the invention.

FlG. 2B is a process flow diagram of an embodiment of the method of the invention.

FIG. 3 is a process flow diagram of an embodiment of the method of the invention.

DETAILED DESCRIPTION Starting Composition (Step (a)): As a starting composition, the method of the present invention uses unsaturated fatty acids, unsaturated fatty esters, salts of unsaturated fatty acids, or a mixture. As used herein the term "unsaturated fatty acid" refers to compounds that

- A - have an alkene chain with a terminal carboxylic acid group. The alkene chain may be a linear or branched and may optionally include one or more functional groups in addition to the carboxylic acid group. For example, some carboxylic acids include one or more hydroxyl groups. The alkene chain typically contains about 4 to about 30 carbon atoms, more typically about 4 to about 22 carbon atoms. In many embodiments, the alkene chain contains 18 carbon atoms (i.e., a Cl 8 fatty acid). The unsaturated fatty acids have at least one carbon-carbon double bond in the alkene chain (i.e., a monounsaturated fatty acid), and may have more than one double bond (i.e., a polyunsaturated fatty acid) in the alkene chain. In exemplary embodiments, the unsaturated fatty acid has from 1 to 3 carbon-carbon double bonds in the alkene chain.

Also useful as starting compositions are unsaturated fatty esters. As used herein the term "unsaturated fatty ester" refers to a compounds that have an alkene chain with a terminal ester group. The alkene chain may be linear or branched and may optionally include one or more functional groups in addition to the ester group. For example, some unsaturated fatty esters include one or more hydroxyl groups in addition to the ester group. Unsaturated fatty esters include "unsaturated monoesters" and "unsaturated polyol esters". Unsaturated monoesters have an alkene chain that terminates in an ester group, for example, an alkyl ester group such as a methyl ester. The alkene chain of the unsaturated monoesters typically contains about 4 to about 30 carbon atoms, more typically about 4 to 22 carbon atoms. In exemplary embodiments, the alkene chain contains 18 carbon atoms (i.e., a Cl 8 fatty ester). The unsaturated monoesters have at least one carbon-carbon double bond in the alkene chain and may have more than one double bond in the alkene chain. In exemplary embodiments, the unsaturated fatty ester has 1 to 3 carbon- carbon double bonds in the alkene chain.

Also useful as a starting composition are metal salts of unsaturated fatty acids (i.e., carboxylate salts of unsaturated fatty acids). The metal salts may be salts of alkali metals (e.g., a group IA metal such as Li, Na, K, Rb, and Cs); alkaline earth metals (e.g., group HA metals such as Be, Mg, Ca, Sr, and Ba); group UIA metals (e.g., B, Al, Ga, In, and Tl); group IVA metals (e.g., Sn and Pb), group VA metals

(e.g., Sb and Bi), transition metals (e.g., Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Zr, Mo, Ru, Rh, Pd, Ag and Cd), lanthanides or actinides.

In many embodiments, the unsaturated fatty acid, ester, or carboxylate salt has a straight alkene chain and can be represented by the general formula:

CH ₃ -(CH ₂ ) _nl -[-(CH ₂ ) _n3 -CH=CH-] _x -(CH ₂ ) _n2 -COOR where:

R is hydrogen (fatty acid), an aliphatic group (fatty ester), or a metal ion (carboxylate salt); n 1 is an integer equal to or greater than O (typically O to 15; more typically O,

3, or 6); n2 is an integer equal to or greater than 0 (typically 2 to 1 1 ; more typically 3, 4, 7, 9, or 1 1); n3 is an integer equal to or greater than 0 (typically 0 to 6; more typically 1); and x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1 to

3). A summary of some unsaturated fatty acids and esters is provided in TABLE A.

TABLE A: Unsaturated Fatty Acids/Esters

Unsaturated monoesters may be alkyl esters (e.g., methyl esters) or aryl esters and may be derived from unsaturated fatty acids or unsaturated glycerides by transesterifying with a monohydric alcohol. The monohydric alcohol may be any monohydric alcohol that is capable of reacting with the unsaturated free fatty acid or unsaturated glyceride to form the corresponding unsaturated monoester. In some embodiments, the monohydric alcohol is a Cl to C20 monohydric alcohol, for example, a Cl to C12 monohydric alcohol, a Cl to C8 monohydric alcohol, or a C l to C4 monohydric alcohol. The carbon atoms of the monohydric alcohol may be arranged in a straight chain or in a branched chain structure, and may be substituted with one or more substituents. Representative examples of monohydric alcohols include methanol, ethanol, propanol (e.g., isopropanol), and butanol.

Transesterification of an unsaturated triglyceride can be represented as follows.

Unsaturated Triglyceride + 3 Alcohol → 1 Glycerol + 3 Monoesters

Depending upon the make-up of the unsaturated triglyceride, the above reaction may yield one, two, or three moles of unsaturated monoester. Transesterification is typically conducted in the presence of a catalyst, for example, alkali catalysts, acid catalysts, or enzymes. Representative alkali transesterification catalysts include NaOH, KOH, sodium and potassium alkoxides (e.g., sodium methoxide), sodium ethoxide, sodium propoxide, sodium butoxide. Representative acid catalysts include sulfuric acid, phosphoric acid, hydrochloric acid, and sulfonic acids. Heterogeneous catalysts may also be used for transesterification. These include alkaline earth metals or their salts such as CaO, MgO, calcium acetate,

barium acetate, natural clays, zeolites, Sn, Ge or Pb, supported on various materials such as ZnO, MgO, TiO ₂ , activated carbon or graphite, and inorganic oxides such as alumina, silica-alumina, boria, oxides of P, Ti, Zr, Cr, Zn, Mg, Ca, and Fe. In exemplary embodiments, the triglyceride is transesterified with methanol (CH ₃ OH) in order to form free fatty acid methyl esters.

In some embodiments, the unsaturated fatty esters are unsaturated polyol esters. As used herein the term "unsaturated polyol ester" refers to compounds that have at least one unsaturated fatty acid that is esterified to the hydroxyl group of a polyol. The other hydroxyl groups of the polyol may be unreacted, may be esterified with a saturated fatty acid, or may be esterified with an unsaturated fatty acid. The fatty acids in the polyol ester may be linear or branched and may optionally have functional groups other than the carboxylic acid such as one or more hydroxyl groups. Examples of polyols include glycerol, 1, 3 propanediol, propylene glycol, erythritol, trimethylolpropane, pentaerythritol, and sorbitol. In many embodiments, unsaturated polyol esters have the general formula:

R (O-Y) _m (OH) _n (O-X) _b

where R is an organic group having a valency of (n+m+b); m is an integer from 0 to (n+m+b- 1), typically 0 to 2; b is an integer from 1 to (n+m+b), typically 1 to 3; n is an integer from 0 to (n+m+b- 1), typically 0 to 2; (n+m+b) is an integer that is 2 or greater; X is -(O)C-(CH ₂ ) _n2 -[-CH=CH-(CH ₂ ) _n3 -] _x -(CH ₂ ) _nl -CH ₃ ;

Y iS -(O)C-R ^' ;

R' is a straight or branched chain alkyl or alkenyl group; nl is an integer equal to or greater than O (typically O to 15; more typically O, 3, or 6); n2 is an integer equal to or greater than 0 (typically 2 to 1 1 ; more typically 3, 4, 7, 9, or 11);

n3 is an integer equal to or greater than 0 (typically 0 to 6; more typically 1); and x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1 to 3).

In many embodiments, the unsaturated polyol esters are unsaturated glycerides. As used herein the term "unsaturated glyceride" refers to a polyol ester having at least one (e.g., 1 to 3) unsaturated fatty acid that is esterified with a molecule of glycerol. The fatty acid groups may be linear or branched and may include pendant hydroxyl groups. In many embodiments, the unsaturated glycerides are represented by the general formula:

CH ₂ A-CHB-CH ₂ C

where -A; -B; and -C are selected from

-OH;

-O(O)C-(CH ₂ ) _n2 -[-CH=CH-(CH ₂ ) _n3 -] _x -(CH ₂ ) _{n I} -CH ₃ ; and -0(O)C-R'; with the proviso that at least one of -A, -B, or -C is -O(O)C-(CH ₂ ) _n2 -[-CH=CH-(CH ₂ ) _n3 -] _x -(CH ₂ ) _n ,-CH ₃

In the above formula:

R ^' is a straight or branched chain alkyl or alkenyl group; nl is an integer equal to or greater than O (typically O to 15; more typically O, 3, or 6); n2 is an integer equal to or greater than O (typically 2 to 1 1 ; more typically 3, 4, 7, 9, or 1 1); n3 is an integer equal to or greater than O (typically O to 6; more typically 1); and x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1 to 3).

Unsaturated glycerides having two -OH groups (e.g., -A and -B are -OH) are commonly known as unsaturated monoglycerides. Unsaturated glycerides having one -OH group are commonly known as unsaturated diglycerides. Unsaturated glycerides having no -OH groups are commonly known as unsaturated triglycerides.

As shown in the formula above, the unsaturated glyceride may include monounsaturated fatty acids, polyunsaturated fatty acids, and saturated fatty acids that are esterified to the glycerol molecule. The main chain of the individual fatty acids may have the same or different chain lengths. Accordingly, the unsaturated glyceride may contain up to three different fatty acids so long as at least one fatty acid is an unsaturated fatty acid.

In many embodiments, useful starting compositions are derived from natural oils such as plant-based oils or animal fats. Representative examples of plant-based oils include canola oil, rapeseed oil, coconut oil, corn oil, cottonseed oil, olive oil, palm oil, peanut oil, safflower oil, sesame oil, soybean oil, sunflower oil, linseed oil, palm kernel oil, tung oil, castor oil, and the like. Representative examples of animal fats include lard, tallow, chicken fat (yellow grease), and fish oil. Other useful oils include tall oil and algae oil.

In many embodiments, the plant-based oil is soybean oil. Soybean oil comprises unsaturated glycerides, for example, in many embodiments about 95% weight or greater (e.g., 99% weight or greater) triglycerides. Major fatty acids making up soybean oil include saturated fatty acids, for example, palmitic acid (hexadecanoic acid) and stearic acid (octadecanoic acid), and unsaturated fatty acids, for example, oleic acid (9-octadecenoic acid), linoleic acid (9, 12-octadecadienoic acid), and linolenic acid (9,12,15-octadecatrienoic acid). Soybean oil is a highly unsaturated vegetable oil with many of the triglyceride molecules having at least two unsaturated fatty acids.

The method of the invention can be used to produce multiple organic acid compounds. As discussed below, the position of the carbon-carbon double bond closest to the carboxylic acid, ester, or carboxylate salt group dictates the chain length of the organic acid compound that is formed by the method of the invention. δ9 Starting Compositions:

In many embodiments, the starting composition comprises a δ9 unsaturated fatty acid, a δ9 unsaturated fatty ester (e.g., monoesters or polyol esters), a δ9 unsaturated fatty acid salt, or a mixture of two or more of the foregoing. δ9 unsaturated starting materials have a carbon-carbon double bond located between the 9 ^th and 10 ^th carbon atoms (i.e., between C9 and C lO) in the alkene chain of the unsaturated fatty acid, ester, or salt. In determining this position, the alkene chain is numbered beginning with the carbon atom in the carbonyl group of the unsaturated fatty acid, ester, or salt. δ9 unsaturated fatty acids, esters, and salts include polyunsaturated fatty acids, esters, or salts (i.e., having more than one carbon-carbon double bond in the alkene chain) so long as one of the carbon-carbon double bonds is located between C9 and C lO. For example, included within the definition of δ9 unsaturated fatty acids, esters, or salts are δ9, 12 unsaturated fatty acids, esters or salts, and δ9, 12, 15 unsaturated fatty acids, esters or salts.

In many embodiments, the δ9 unsaturated starting materials have a straight alkene chain and may be represented by the general structure:

CH ₃ -(CH ₂ ) _nl -[-(CH ₂ ) _n3 -CH=CH-] _x -(CH ₂ ) ₇ -COOR where

R is hydrogen (fatty acid), an aliphatic group (fatty monoester) or a metal ion (carboxylate salt); nl is an integer equal to or greater than 0 (typically 0 to 6; more typically 0, 3, 6); n3 is an integer equal to or greater than 0 (typically 1); and x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1 to 3).

In exemplary embodiments, the δ9 unsaturated starting materials have a total of 18 carbons in the alkene chain. Examples include

CH ₃ -(CH ₂ ) ₇ -CH=CH-(CH ₂ ) ₇ -COOR;

CH ₃ -(CH ₂ ) ₄ -CH=CH-CH ₂ -CH=CH-(CH ₂ ) ₇ -COOR; and CH ₃ -CH ₂ -CH<:H-CH ₂ -CH<:H-CH ₂ -CH=CH-(CH ₂ ) ₇ -COOR.

where R is hydrogen (fatty acid), an aliphatic group (fatty monoester) or a metal ion (fatty acid salt);

δ9 unsaturated fatty esters may be monoesters or polyol esters. In many embodiments, the δ9 unsaturated polyol esters have the general structure

CH ₂ A-CHB-CH ₂ C

where -A; -B; and -C are independently selected from

-OH;

-0(O)C-R'; and

-O(O)C-(CH ₂ ) ₇ -[-CH=CH-(CH ₂ ) _n3 -] _x- -(CH ₂ ) _n ,-CH ₃ ; with the proviso that at least one of -A, -B, or -C is -O(O)C-(CH ₂ ) ₇ -[-CH=CH-(CH ₂ ) _n3 -] _x- -(CH ₂ ) _nl -CH ₃ .

In the above formula:

R' is a straight or branched chain alkyl or alkenyl group; nl is an integer equal to or greater than O (typically O to 6; more typically O, 3, 6); n3 is an integer equal to or greater than O (typically 1); and x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1 to 3).

In exemplary embodiments, the starting composition comprises one or more Cl 8 fatty acids, for example, oleic acid (i.e., 9-octadecenoic acid), linoleic acid (i.e., 9, 12-octadecadienoic acid), and linolenic acid (i.e., 9, 12, 15-octadecatrienoic acid). In other exemplary embodiments, the starting composition comprises one or more Cl 8 fatty esters, for example, methyl oleate, methyl linoleate, and methyl linolenate. In yet another exemplary embodiment, the starting composition comprises an unsaturated glyceride comprising δ9 fatty acids, for example, C 18 δ9 fatty acids. δ9 starting compositions may be derived, for example, from vegetable oils such as soybean oil, rapeseed oil, corn oil, sesame oil, cottonseed oil, sunflower oil,

canola oil, safflower oil, palm oil, palm kernel oil, linseed oil, castor oil, olive oil, peanut oil, and the like. Since these vegetable oils yield predominately in glyceride form, the oils are typically processed (e.g., by transesterification) to yield unsaturated free fatty esters, unsaturated free fatty acids, or carboxylate salts thereof. δ9 starting materials may also be derived from tung oil which typically contains oleic acid, linoleic acid, and eleostearic acid (C 18; δ9, 1 1 , 13) in glyceride form. δ9 starting materials may also be derived from tall oil, fish oil, lard, and tallow. δ5 Starting Compositions:

Also useful as a starting composition in the methods of the present invention are δ5 unsaturated fatty acids, esters, or salts. As used herein "δ5" refers to unsaturated fatty acids, esters, or salts having a carbon-carbon double bond located between the 5th and 6th carbon atom in the alkene chain of the unsaturated fatty acid, ester, or salt. In some embodiments, δ5 unsaturated fatty acids, esters, and salts have the general structure:

CH ₃ -(CH ₂ ) _nl -[-(CH ₂ ) _n3 -CH=CH-] _x -(CH ₂ ) ₃ -COOR where

R is hydrogen (fatty acid), an aliphatic group (fatty monoester) or a metal ion (carboxylate salt); nl is an integer equal to or greater than 0 (typically 1 to 15; more typically 1, 13, or 15); n3 is an integer equal to or greater than 0 (typically 0 to 6; more typically 0 or 6); and x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1 to 2).

The δ5 unsaturated fatty esters may be monoesters or polyol esters (e.g., unsaturated glycerides). In many embodiments, the δ5 unsaturated polyol esters have the general structure: CH ₂ A-CHB-CH ₂ C

where -A; -B; and -C are independently selected from

-OH;

-0(O)C-R ^' ; and

-O(O)C-(CH ₂ ) ₃ -[-CH-CH-(CH ₂ ) _n3 -] _x -(CH ₂ ) _nl -CH ₃ ; with the proviso that at least one of -A, -B, or -C is -O(O)C-(CH ₂ ) ₃ -[-CH=CH-(CH ₂ ) _n3 -] _x -(CH ₂ ) _nl CH ₃ .

In the above formula:

R' is a straight or branched chain alkyl or alkenyl group; nl is an integer equal to or greater than O (typically 1 to 15; more typically 1 , 13, or 15); n3 is an integer equal to or greater than O (typically O to 6; more typically O or 6); and x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1 to 2).

δ5 starting compositions may be derived, for example, from meadowfoam oil which contains a twenty carbon monounsaturated fatty acid (C20: 1 ; δ5) in glyceride form. δ5 starting compositions may also be derived from fish oil which typically contains eicosapentaenoic acid (C20:5; δ5, 8, 1 1 , 14, 17) in glyceride form.

δ6 Starting Compositions: Also useful as a starting composition in the methods of the present invention are δ6 unsaturated fatty acids, esters, or salts. As used herein "δ6" refers to unsaturated fatty acids, esters, or salts having a carbon-carbon double bond located between the 6th and 7th carbon atom in the alkene chain of the unsaturated fatty acid, ester, or salt. In some embodiments, δ6 unsaturated fatty acids, esters, and salts have the general structure:

CH ₃ -(CH ₂ ) _{n l} -[-(CH ₂ ) _n3 -CH=CH-] _x -(CH ₂ ) ₄ -COOR where

R is hydrogen (fatty acid), an aliphatic group (fatty monoester) or a metal ion (carboxylate salt); nl is an integer equal to or greater than O (typically O to 10); n3 is an integer equal to or greater than O; (typically 0); and

x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1).

The δ6 unsaturated fatty esters may be monoesters or polyol esters (e.g., unsaturated glycerides). In many embodiments, the δ6 unsaturated polyol esters have the general structure:

CH ₂ A-CHB-CH ₂ C

where -A; -B; and -C are independently selected from -OH;

-0(O)C-R'; and

-O(O)C-(CH ₂ ) ₄ -[-CH=CH-(CH ₂ ) _n3 -] _x -(CH ₂ ) _n ,-CH ₃ ; with the proviso that at least one of -A, -B, or -C is

-O(O)C-(CH ₂ ) ₄ -[-CH=CH-(CH ₂ ) _n3 -] _x -(CH ₂ ) _nl -CH ₃ . In the above formula:

R' is a straight or branched chain alkyl or alkenyl group; nl is an integer equal to or greater than O (typically O to 10); n3 is an integer equal to or greater than O; (typically O); and x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1).

δ6 starting compositions may be derived from coriander oil which contains an 18 carbon unsaturated fatty acid (C 18:1 ; δ6) in glyceride form. δl 1 Starting Compositions:

Also useful as a starting composition in the methods of the present invention are δl 1 unsaturated fatty acids, esters, or salts. As used herein "δl 1" refers to unsaturated fatty acids, esters, or salts having a carbon-carbon double bond located between the 1 1 ^th and 12 ^th carbon atom in the alkene chain of the unsaturated fatty acid, ester, or salt. In some embodiments, δl 1 unsaturated fatty acids, esters, and salts have the general structure:

CH ₃ -(CH ₂ )n,-[-(CH ₂ ) _n3 -CH=CH-] _x -(CH ₂ ) ₉ -COOR where

R is hydrogen (fatty acid), an aliphatic group (fatty monoester) or a metal ion (carboxylate salt); nl is an integer equal to or greater than 0 (typically 0 to 7; more typically 7); n3 is an integer equal to or greater than 0 (typically 0); and x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1).

The δl 1 unsaturated fatty esters may be monoesters or polyol esters (e.g., unsaturated glycerides). In many embodiments, the δl 1 unsaturated polyol esters have the general structure:

CH ₂ A-CHB-CH ₂ C where -A; -B; and -C are independently selected from -OH;

-0(O)C-R'; and -O(O)C-(CH ₂ ) ₉ -[-CH=CH-(CH ₂ ) _n3 -] _x -(CH ₂ ) _{n l} CH ₃ ; with the proviso that at least one of -A, -B, or -C is

-O(O)C-(CH ₂ ) ₉ -[-CH=CH-(CH ₂ ) _n3 -] _x -(CH ₂ ) _nl CH ₃ .

In the above formula: R' is a straight or branched chain alkyl or alkenyl group; nl is an integer equal to or greater than 0 (typically 0 to 7; more typically 7); n3 is an integer equal to or greater than 0 (typically 0); and x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1).

Sources of δl 1 starting compositions include camelina oil which contains gondoic acid (C20: l δl 1) at approximately 15% of the fatty acid composition. δ13 Starting Compositions:

Also useful as a starting composition in the methods of the present invention are δ 13 unsaturated fatty acids, esters, or salts. As used herein "δ13" refers to unsaturated fatty acids, esters, or salts having a carbon-carbon double bond located between the 13 ^th and 14 ^th carbon atom in the alkene chain of the unsaturated fatty

acid, ester, or salt. In some embodiments, δ13 unsaturated fatty acids, esters, and salts have the general structure:

CH ₃ -(CH ₂ ) _nl -[-(CH2)n3-CH=CH-] _x -(CH ₂ ), ,-COOR where

R is hydrogen (fatty acid), an aliphatic group (fatty monoester) or a metal ion (carboxylate salt); nl is an integer equal to or greater than 0 (typically 7); n3 is an integer equal to or greater than 0 (typically 0) x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1).

The δ13 unsaturated fatty esters may be monoesters or polyol esters (e.g., unsaturated glycerides). In many embodiments, the δ13 unsaturated polyol esters have the general structure CH ₂ A-CHB-CH ₂ C where -A; -B; and -C are independently selected from -OH;

-0(O)C-R'; and

-0(O)C-(CH ₂ ), ,-[-CH=CH-(CH ₂ ) _n3 -] _x -(CH ₂ ) _{n l} -CH ₃ ; with the proviso that at least one of -A, -B, or -C is

-O(O)C-(CH ₂ ), ,-[-CH=CH-(CH ₂ ) _n3 -] _x -(CH ₂ ) _nl -CH ₃ . In the above formula:

R' is a straight or branched chain alkyl or alkenyl group; nl is an integer equal to or greater than O (typically 7); n3 is an integer equal to or greater than O (typically O) x is an integer equal to or greater than 1 (typically 1 to 6, more typically 1).

Sources of δl 3 starting compositions include crambe oil, fish oil, and high erucic acid rapeseed oil which are high in erucic acid (C22: 1 δ13) in glyceride form. Other useful starting compositions include, for example, δ8 and δ4 starting materials. δ4 starting materials may be obtained, for example, from fish oil which typically includes an amount of docosahexaenoic acid (C22:6; δ4, 7, 10, 13, 16, 19).

δ8 starting materials may also be obtained from fish oil which typically includes an amount of eicosatetraenoic acid (C20:4; δ8, 1 1 , 14, 17).

A summary of some useful starting compositions is provided in TABLE B.

TABLE B

Cross-Metathesis (Step (bϊ):

According to the method of the invention, the starting composition is cross- metathesized with a short-chain olefin in the presence of a metathesis catalyst to form cross-metathesis products comprising: (i) one or more olefin compounds; and

(ii) one or more acid-, ester-, or carboxylate salt-functionalized alkenes having at least one carbon-carbon double bond.

Short-chain olefins are short chain length organic compounds that have at least one carbon-carbon double bond. In many embodiments, the short chain olefins have between about 4 and about 9 carbon atoms. Short chain olefins can be represented by the structure (11):

R ⁷ R ⁸ C=CR ⁹ R ¹⁰

(H) where R ⁷ , R ⁸ , R ⁹ , and R ¹⁰ are each, independently, hydrogen or an organic group, with the proviso that at least one of R ⁷ or R ⁸ is an organic group.

The organic group may be an aliphatic group, an alicyclic group, or an aromatic group. Organic groups may optionally include heteroatoms (e.g., O, N, or S atoms), as well as functional groups (e.g., carbonyl groups). The term aliphatic group means a saturated or unsaturated, linear or branched, hydrocarbon group. This term is used to encompass alkyl groups. The term alkyl group means a monovalent, saturated, linear, branched, or cyclic hydrocarbon group. Representative examples of alkyl groups include methyl, ethyl, propyl (n-propyl or i-propyl), butyl (n-butyl or t-butyl), pentyl, hexyl, and heptyl. An alicyclic group is an aliphatic group arranged in one or more closed ring structures. The term is used to encompass saturated (i.e., cycloparaffins) or unsaturated (cycloolefins or cycloacetylenes) groups. An aromatic or aryl group is an unsaturated cyclic hydrocarbon having a conjugated ring structure. Included within aromatic or aryl groups are those possessing both an aromatic ring structure and an aliphatic or alicyclic group. In many embodiments, the short-chain olefin is a short-chain internal olefin.

Short-chain internal olefins may be represented by structure (II):

R ⁷ R ⁸ C=CR ⁹ R ¹⁰

(II) where R ⁷ , R ⁸ , R ⁹ , and R ¹⁰ are each, independently, hydrogen or an organic group, with the proviso that at least one of R ⁷ or R ⁸ is an organic group, and at least one of R ⁹ or R ¹⁰ is an organic group.

Short-chain internal olefins may be symmetric or asymmetric. Symmetric short-chain internal olefins having one carbon-carbon double bond may be represented by structure (H-A): R ⁷ CH=CHR ⁹

(H-A) where -R ⁷ and -R ⁹ are same organic group.

Representative examples of symmetric short-chain internal olefins include 2- butene, 3-hexene, and 4-octene. In some embodiments, the short-chain internal olefin is asymmetric. Representative examples of asymmetric short-chain internal olefins include 2-pentene, 2-hexene, 2-heptene, 3-heptene, 2-octene, 3-octene, 2- nonene, 3-nonene, and 4-nonene.

In many embodiments, symmetric short-chain internal olefins are preferred for cross-metathesis because the cross-metathesis products that result will include fewer products than if an asymmetric short-chain internal olefin is used for cross- metathesis. For example, as shown below, when a first double-bond containing compound (i.e., A=B) is cross-metathesized with a symmetric short-chain internal olefin (i.e., represented by C=C), two cross-metathesis products are produced. By contrast, when the same double-bond containing compound is cross-metathesized with an asymmetric short-chain internal olefin (i.e., represented by C=D), four cross-metathesis products are produced.

Metathesis of Symmetric Short-chain Internal Olefin (C=C) A=B + C=C < ^■ > A=C + B=C

Metathesis of Asymmetric Short-chain Internal Olefin (C=D): A=B + C=D <-> A=C + B=C + A=D + B=D

In some embodiments, the short-chain olefin is an α-olefin. Alpha olefins are included in general structure (II) when R ⁷ , R ⁸ , and R ⁹ are all hydrogen. Representative α-olefin are shown in general structure (H-B):

CH ₂ =CH-R ¹⁰

(H-B) where -R ¹⁰ is an organic group.

Representative -R ¹⁰ groups include -(CH ₂ ) _O -CH ₃ , where n ranges from 0 to 6. Exemplary alpha olefin compounds include 1 -propene, 1 -butene, 1 -pentene, 1 - hexene, 1-heptene, 1 -octene, and 1 -nonene. Metathesis Catalysts: Metathesis reactions proceed in the presence of a catalytically effective amount of a metathesis catalyst. The term "metathesis catalyst" includes any catalyst or catalyst system which catalyzes the olefin metathesis reaction.

Any known or future-developed metathesis catalyst may be used, alone or in combination with one or more additional catalysts, in accordance with embodiments of the present method. Exemplary metathesis catalysts used can include metal carbene catalysts based upon transition metals, such as ruthenium. Exemplary ruthenium-based metathesis catalysts include those represented by structures 12 (commonly known as Grubbs's catalyst), 14 and 16, where Ph is phenyl, Mes is mesityl, and Cy is cyclohexyl.

12 14 16

Structures 18, 20, 22, 24, 26, and 28, illustrated below, represent additional ruthenium-based metathesis catalysts, where Ph is phenyl, Mes is mesityl, py is pyridine, Cp is cyclopentyl, and Cy is cyclohexyl. Techniques for using catalysts 12, 14, 16, 18, 20, 22, 24, 26, and 28, as well as additional related metathesis catalysts, are known in the art.

18 20 22

Catalysts C627, C682, C697, C712, and C827 are additional ruthenium- based catalysts, where Cy is cyclohexyl in C827.

C627

C712

C697 C682

Additional exemplary metathesis catalysts include, without limitation, metal carbene complexes selected from the group consisting of molybdenum, osmium,

chromium, rhenium, and tungsten. The term "complex" refers to a metal atom, such as a transition metal atom, with at least one ligand or complexing agent coordinated or bound thereto. Such a ligand typically is a Lewis base in metal carbene complexes useful for alkene, alkyne or alkene-metathesis. Typical examples of such ligands include phosphines, halides and stabilized carbenes. Some metathesis catalysts may employ plural metals or metal co-catalysts (e.g. a catalyst comprising a tungsten halide, a tetraalkyl tin compound, and an organoaluminum compound).

An immobilized catalyst can be used for the metathesis process. An immobilized catalyst is a system comprising a catalyst and a support, the catalyst associated with the support. Exemplary associations between the catalyst and the support may occur by way of chemical bonds or weak interactions (e.g. hydrogen bonds, donor acceptor interactions) between the catalyst, or any portions thereof, and the support or any portions thereof. Support is intended to include any material suitable to support the catalyst. Typically, immobilized catalysts are solid phase catalysts that act on liquid or gas phase reactants and products. Exemplary supports are polymers, silica or alumina. Such an immobilized catalyst may be used in a flow process. An immobilized catalyst can simplify purification of products and recovery of the catalyst so that recycling the catalyst may be more convenient.

The metathesis process for producing industrial chemicals can be conducted under any conditions adequate to produce the desired metathesis product or products. For example, stoichiometry, atmosphere, solvent, temperature and pressure can be selected to produce a desired product and to minimize undesirable byproducts. The metathesis process may be conducted under an inert atmosphere. Similarly, if an olefin reagent is supplied as a gas, an inert gaseous diluent can be used. The inert atmosphere or inert gaseous diluent typically is an inert gas, meaning that the gas does not interact with the metathesis catalyst to substantially impede catalysis. For example, particular inert gases are selected from the group consisting of helium, neon, argon, nitrogen and combinations thereof.

Similarly, if a solvent is used, the solvent chosen may be selected to be substantially inert with respect to the metathesis catalyst. For example, substantially inert solvents include, without limitation, aromatic hydrocarbons, such as benzene, toluene, xylenes, etc.; halogenated aromatic hydrocarbons, such as chlorobenzene

and dichlorobenzene; aliphatic solvents, including pentane, hexane, heptane, cyclohexane, etc.; and chlorinated alkanes, such as dichloromethane, chloroform, dichloroethane, etc.

In certain embodiments, a ligand may be added to the metathesis reaction mixture. In many embodiments using a ligand, the ligand is selected to be a molecule that stabilizes the catalyst, and may thus provide an increased turnover number for the catalyst. In some cases the ligand can alter reaction selectivity and product distribution. Examples of ligands that can be used include Lewis base ligands, such as, without limitation, trialkylphosphines, for example tricyclohexylphosphine and tributyl phosphine; triarylphosphines, such as triphenylphosphine; diarylalkylphosphines, such as, diphenylcyclohexylphosphine; pyridines, such as 2,6-dimethylpyridine, 2,4,6-trimethylpyridine; as well as other Lewis basic ligands, such as phosphine oxides and phosphinites. Additives may also be present during metathesis that increase catalyst lifetime. Using currently known catalysts, the metathesis processing temperature may largely be a rate-dependent variable where the temperature is selected to provide a desired product at an acceptable production rate. The selected temperature may be greater than about -40°C, may be more than about -20°C, and is generally selected to be more than about O ⁰ C or more than about 20°C. Generally, the process temperature may be no more than about 150°C, and may be no more than about 120°C. Thus, an exemplary temperature range for the metathesis reaction may be from about 20°C to about 120 ⁰ C. Lower temperatures can be used, for example, to minimize the production of undesired impurities or to favor a particular reaction pathway. Any useful amount of the selected metathesis catalyst can be used in the process. For example, the molar ratio of the unsaturated polyol ester to catalyst may range from about 5: 1 to about 10,000,000: 1 or from about 50: 1 to 500,000: 1.

The metathesis process steps (i.e., step (b) and step (d)) can be conducted under any desired pressure. For example, the cross-metathesis step (b) is typically conducted at a pressure ranging from about 10 kPa to about 7000 kPa or from about 100 kPa to about 3000 kPa. In some embodiments, it is preferred to conduct the self-metathesis step (i.e., step (d)) at low pressure, for example, about 0.01 kPa to

about 100 kPa, more typically about 0.01 kPa to about 50 kPa. By conducting the self-metathesis at low pressure, the low boiling point olefin products (e.g., the short- chain internal olefin or alpha olefin) that are formed during the cross-metathesis reaction can be easily separated from the higher boiling point functionalized olefin products (e.g., the one or more diacid olefins, diester olefins, or disalt olefins). This separation is advantageous for two reasons. First, in an integrated process, the separation of the short-chain internal olefin product allows this material to be recycled back to the reactor where the cross-metathesis step (i.e., step (b)) is being conducted. Second, the removal of the olefin products from the functionalized olefin products drives the equilibrium of the self-metathesis reaction (i.e., step (d)) to the formation of more functionalized olefin product. This results in a higher yield of the desired functionalized olefin product.

The metathesis reaction may be catalyzed by a system containing both a transition and a non-transition metal component. The most active and largest number of two-part catalyst systems are derived from Group VI A transition metals, for example, tungsten and molybdenum. Separation Step (step (cϊ):

After cross-metathesis with a short-chain olefin, at least a portion of the acid-, ester-, or carboxylate salt-functionalized alkene is separated from the remaining cross-metathesis products. If cross-metathesis is conducted on an unsaturated glyceride starting composition the resulting cross-metathesis products should be transesterified prior to separation. This allows the separation step to separate the ester-functionalized alkene from any ester functionalized alkane that may be present in the transesterification products. Useful techniques for separating the acid-, ester-, or carboxylate salt- functionalized alkene from the remaining cross-metathesis products include, for example, distillation, reactive distillation, chromatography, fractional crystallization, membrane separation, liquid/liquid extraction, or a combination thereof.

In many embodiments, the acid-, ester-, or carboxylate salt-functionalized alkene can be purified to a high degree using one or more of the above-described techniques. For example, the acid-, ester-, or carboxylate salt-functionalized alkene can be purified to a level of 90% wt. or greater (e.g., 95% wt. or greater, 96% wt. or

greater, 97% wt. or greater, 98% wt. or greater, 99% wt. or greater, 99.5% wt. or greater, or 99.9% wt. or greater). Using the method of the invention, a high purity functionalized alkene intermediate can be obtained using one or more conventional separation processes. Achieving a high purity functionalized alkene intermediate allows for the production of a high purity products from the methods of the invention For example, in some embodiments, the product has a purity of 90% wt. or greater (e.g., 95% wt. or greater, 96% wt. or greater, 97% wt. or greater, 98% wt. or greater, 99% wt. or greater, 99.5% wt. or greater, or 99.9% wt. or greater). Self or Cross-Metathesis Step (step (dV): In some embodiments, after separation, the isolated acid-, ester-, or salt- functionalized alkene is self-metathesized in the presence of a metathesis catalyst to form a composition comprising one or more diacid alkenes, diester alkenes, or dicarboxylate salt alkenes. For example, when a δ9 acid-functionalized starting composition is used and is cross-metathesized with 2-butene, the resulting acid- functionalized alkene has the structure HOOC-(CH ₂ ) ₇ -CH=CH-CH ₃ . After separation, self-metathesis of the acid-functionalized alkene yields an unsaturated Cl 8 diacid and 2-butene according to the formula below:

2 HOOC-(CH ₂ ) ₇ -CH=CH-CH ₃ → HOOC-(CH ₂ ) ₇ -CH=CH-(CH ₂ ) ₇ -COOH + CH ₃ -CH-CH-CH ₃

In similar fashion, when a δ9 methyl ester-functionalized starting composition is used and is cross-metathesized with 2-butene, the resulting methyl ester-functionalized alkene has structure CH ₃ OOC-(CH ₂ ) ₇ -CH=CH-CH ₃ . SeIf- metathesis of the ester-functionalized olefin yields an unsaturated C 18 diester and 2- butene according to the formula below:

2 CH ₃ OOC-(CH ₂ ) ₇ -CH=CH-CH ₃ → CH ₃ OOC-(CH ₂ ) ₇ -CH=CH-(CH ₂ ) ₇ -COOCH ₃ +

CH ₃ -CH=CH-CH ₃

In another embodiment, a δ5 acid-functionalized starting composition is used and is cross-metathesized with 2-butene to provide an acid-functionalized

alkene having the structure HOOC-(CH ₂ ) ₃ -CH=CH-CH ₃ . Self-metathesis of the acid-functionalized alkene yields an unsaturated ClO diacid and 2-butene according to the formula below:

2 HOOC-(CH ₂ ) ₃ -CH=CH-CH ₃ → HOOC-(CH ₂ ) ₃ -CH=CH-(CH ₂ ) ₃ -COOH +

CH ₃ -CH=CH-CH ₃

In another embodiment, a δ6 acid-functionalized starting composition is used and is cross-metathesized with 2-butene to provide an acid-functionalized alkene having the structure HOOC-(CH ₂ ) ₄ -CH=CH-CH ₃ . Self-metathesis of the ester- functionalized alkene yields an unsaturated C 12 diacid and 2-butene according to the formula below:

2 HOOC-(CH ₂ ) ₄ -CH=CH-CH ₃ → HOOC-(CH ₂ ) ₄ -CH=CH-(CH ₂ ) ₄ -COOH +

CH ₃ -CH=CH-CH ₃

In another embodiment, a δ13 acid-functionalized starting composition is used and is cross-metathesized with 2-butene to provide an acid-functionalized alkene having the structure HOOC-(CH ₂ ), ,-CH=CH-CH ₃ . Self-metathesis of the ester- functionalized alkene yields an unsaturated C26 diacid and 2-butene according to the formula below:

2 HOOC-(CH ₂ ), ,-CH=CH-CH ₃ → HOOC-(CH ₂ ), , -CH=CH-(CH ₂ ), ,- COOH +

CH ₃ -CH=CH-CH ₃

Other self-metathesis reactions would follow the above reaction scheme. In some embodiments, after separation, the isolated acid-, ester-, or carboxylate salt-functionalized alkene is cross-metathesized with a second functionalized alkene compound in the presence of a metathesis catalyst to form a bifunctional organic compound. Exemplary bifunctional organic compounds

obtainable by this method include diacids, acid/esters, acid/amines, acid/alcohols, acid/aldehydes, acid/ketones, acid/halides, acid/nitriles, as well as diesters, ester/amines, ester/alcohols, ester/aldehydes, ester/ketones, ester/halides, and ester/nitriles. In many embodiments, after cross-metathesis, the resulting bifunctional organic comound is hydrogenated in order to saturate the double-bond that is present in the bifunctional compound. For example, starting with fatty acids δ5 and higher, alpha,omega-diacids from C7 to Cl 8 and higher can be made. Similarly, omega-hydroxycarboxylic acids and omega-aminocarboxylic acids from C7 to Cl 8 and higher can be made. The second functional ized alkene compound has at least one carbon-carbon double bond and has at least one organic functional group. Examples of organic functional groups include carboxylic acids, esters, amines, amides, halogens, aldehydes, nitriles, isocyanates, ketones, epoxides, and alcohols. In many embodiments, the second functionalized alkene has the general structure (III):

R ^l2 -CH=CH-(CH ₂ ) _n -R ¹³

(III) where n is 0 or an integer (typically 1 to 20); -R ¹² is hydrogen, an alkyl group, an aryl group, or -(CH ₂ ) _n -R ¹³ ;

-R ¹³ is a functional group (typically -COOH, -COOR ¹⁴ , -COH; - COR ¹⁴ ; -CONH ₂ ; -C≡N; -NH ₂ ; -OH; or -X); -R ¹⁴ is alkyl group or an aryl group; and -X is a halogen (typically Cl, F, Br, or I).

Examples of second functionalized alkene compounds include 2-butene-l,4- dioic acid (HOOCCH=CHCOOH), acrylic acid (CH=CHCOOH), 2-butenoic acid (CH ₃ CH=CHCOOH), 2-pentenoic acid (CH ₃ CH ₂ CH=CHCOOH), 2-hexenoic acid (CH ₃ CH ₂ CH ₂ CH=CHCOOH), 3-hexenedioc acid (HOOCCH ₂ CH=CHCH ₂ COOH), the dimethyl ester of 3-hexenedioc acid (CH ₃ OOCCH ₂ CH=CHCH ₂ COOCH ₃ ), 3- hexenoic acid (HOOCCH ₂ CH=CHCH ₂ CH ₃ ), the methyl ester of 3-hexenoic acid (CH ₃ OOCCH ₂ CH=CHCH ₂ CH ₃ ), 3-pentenoic acid (HOOCCH ₂ CH=CHCH ₃ ), methyl

ester of 3-pentenoic acid (CH ₃ OOCCH ₂ CH=CHCH ₃ ), 4-pentenoic acid, 4-hexenoic acid, 4-heptenoic acid, 4-octenoic acid and its esters, 4-octene-l,8-dioic acid and its esters, 5-hexenoic acid, l -bromo-3 hexene, 3-butenal diethyl acetal, 5-heptenoic acid, 5-octenoic acid and its esters, 5-decene-l,10-dioic acid and its esters, 6- heptenoic acid, 6-octenoic acid, 6-nonenoic acid, 6-decenoic acid and its esters, 6- dodecene-l ,12-dioic acid and its esters, 7-octenoic acid, 7-nonenoic acid, 7-decenoic acid, 7-undecenoic acid, and 7-dodecenoic acid and its esters.

Additional examples of second functionalized alkene compounds include allyl alcohol, 2-butenol, 3-buten-l-ol, 2-penten-l-ol, 3-penten-l-ol, 4-penten-l -ol, 2- hexen- 1 -ol, 3-hexen- 1 -ol, 4-hexen- 1 -ol, 5-hexen- 1 -ol, and the like; buten- 1 ,4-diol, 2-penten-l,5-diol, 2-hexen-l,6-diol, 3-hexen- 1,6-diol, and the like; allyl amine, 1- amino-2-butene, l-amino-3-butene, 1 -amino-2-pentene, l-amino-3-pentene, 1 - amino-4-pentene, l-amino-2-hexene, l-amino-3-hexene, l-amino-4 hexene, 1 - amino-5-hexene, and the like; l ,4-diamino-2-butene, l,5-diamino-2-pentene, 1 ,6- diamino-2-hexene, l ,6-diamino-3-hexene, and the like; l-chloro-2-propene (i.e., allyl chloride), 1 -chloro-2-butene, l-chloro-3-butene, 1 -chloro-2-pentene, 1-chloro- 3-pentene, l-chloro-4-pentene, l-chloro-2-hexene, l-chloro-3-hexene, l -chloro-4- hexene, l-chloro-5-hexene, and the like (including the F, Br, or I analogs); 1,4- dichloro-2-butene (CI-CH ₂ -CH=CH-CH ₂ -CI), l,5-dichloro-2-pentene, 1 ,6-dichloro- 2-hexene, l,6-dichloro-3-hexene, and the like (including the F, Br, or I analogs); acrolein (propenal), 2-butenal, 3-butenal, 2-pentenal, 3-pentenal, 4-pentenal, 2- hexenal, 3-hexenal, 4-hexenal, 5-hexenal, and the like; 2-buten-l ,4-dial, 2-penten- 1,5-dial, 2-hexen-l,6-dial, 3-hexen- 1 ,6-dial, and the like; acrylonitrile (cyanoethylene), 1-cyano-l-propene, 1 -cyano-2-propene, 1 -cyano- 1 -butene, 1- cyano-2-butene, l-cyano-3 -butene, 1 -cyano- 1 -pentene, l-cyano-2-pentene, 1-cyano- 3-pentene, and the like; 1 ,2-dicyanoethylene, 1,3-dicyanopropene, 1,4-dicyano-l- butene, 1 ,4-dicyano-2-butene, and the like.

In exemplary embodiments, the second functionalized alkene is symmetric about its carbon-carbon double bond. That is, the group -R ¹² is the same as group - (CH ₂ ) _n -R ¹³ . Advantageously, when the second functionalized alkene is symmetric, the number of products formed in the cross-metathesis reaction is reduced as compared to cross-metathesis reactions where the second functionalized alkene is

asymmetric. This may provide for higher yields and/or easier separation of the desired bifunctional compound. Representative examples of symmetric functionalized alkenes include maleic acid (HO ₂ CCH=CHCO ₂ H) and esters thereof, 3-hexenedioc acid (HO ₂ CCH ₂ CH=CHCH ₂ CO ₂ H) and esters thereof (e.g., the dimethyl ester of 3-hexenedioc acid (CH ₃ O ₂ CCH ₂ CH=CHCH ₂ CO ₂ CH ₃ )), 4-octene- 1,8-dioic acid and esters thereof, 5-decene-l,10-dioic acid and esters thereof, and 6- dodecene-l ,12-dioic acid esters.

In an exemplary embodiment, a δ9 acid-functionalized starting composition is used and is cross-metathesized with 2-butene, providing an acid-functionalized alkene having the structure HO ₂ C-(CH ₂ ) ₇ -CH=CH-CH ₃ . After separation, the acid- functionalized alkene is cross-metathesized with 3-hexenedioc acid (HO ₂ CCH ₂ CH=CHCH ₂ CO ₂ H) in the presence of a metathesis catalyst. The cross- metathesis yields an unsaturated C 12 diacid according to the formula below:

HO ₂ C-(CH ₂ ) ₇ -CH=CH-CH ₃ + HO ₂ CCH ₂ CH=CHCH ₂ CO ₂ H →

HO ₂ C-(CH ₂ ) ₇ -CH=CH-CH ₂ -CO ₂ H + CH ₃ -CH=CHCH ₂ CO ₂ H

Optionally, the unsaturated C 12 diacid may be hydrogenated to produce the corresponding saturated C 12 diacid. In another exemplary embodiment, a δ9 acid-functionalized starting composition is used and is cross-metathesized with 2-butene, providing an acid- functionalized alkene having the structure HO ₂ C-(CH ₂ ) ₇ -CH=CH-CH ₃ . After separation, the acid-functionalized alkene is cross-metathesized with maleic acid (HO ₂ C-CH=CH-CO ₂ H) in the presence of a metathesis catalyst. The cross- metathesis yields an unsaturated C 1 1 diacid according to the formula below:

HO ₂ C-(CH ₂ ) ₇ -CH=CH-CH ₃ + HO ₂ C-CH=CH-CO ₂ H → HO ₂ C-(CH ₂ ) ₇ -CH=CH-CO ₂ H + CH ₃ -CH=CH-CO ₂ H

Other examples of bifunctional organic products that may be made using the method of the invention are summarized in TABLES C-D.

TABLE C

TABLE D

Optionally, the aboye-listed unsaturated compounds may be hydrogenated to form the corresponding saturated compounds. Hydrogenation Catalysts

After self- or cross-metathesis (i.e., step (d)), the resulting alkene may be hydrogenated to remove the carbon-carbon double bond. Hydrogenation is typically conducted by exposing the alkene to H ₂ gas in the presence of a hydrogenation catalyst. The principal component of the catalyst useful for the hydrogenation is selected from metals from the group consisting of palladium, ruthenium, rhenium, rhodium, iridium, platinum, nickel, cobalt, copper, iron, osmium; compounds thereof; and combinations thereof.

The catalyst may be supported or unsupported. A supported catalyst is one in which the active catalyst agent is deposited on a support material by a number of methods, such as spraying, soaking or physical mixing, followed by drying, calcination, and if necessary, activation through methods such as reduction or oxidation. Materials frequently used as a support are porous solids with high total surface areas (external and internal), which can provide high concentrations of active sites per unit weight of catalyst. The catalyst support may enhance the function of the catalyst agent. A supported metal catalyst is a supported catalyst in which the catalyst agent is a metal.

A catalyst that is not supported on a catalyst support material is an unsupported catalyst. An unsupported catalyst may be platinum black or a Raney™ (W. R. Grace & Co., Columbia, MD) catalyst. Raney™ catalysts have a high surface area due to selectively leaching an alloy containing the active metal(s) and a leachable metal (usually aluminum). Raney® catalysts have high activity due to the higher specific area and allow the use of lower temperatures in hydrogenation reactions. The active metals of Raney™ catalysts include nickel, copper, cobalt, iron, rhodium, ruthenium, rhenium, osmium, iridium, platinum, palladium; compounds thereof; and combinations thereof.

The catalyst support useful herein can be any solid, inert substance including, but not limited to, oxides such as silica, alumina and titania; barium sulfate; calcium carbonate; and carbons. The catalyst support can be in the form of powder, granules, pellets, or the like.

A preferred support material of the invention is selected from the group consisting of carbon, alumina, silica, silica-alumina, silica-titania, titania, titania-

alumina, barium sulfate, calcium carbonate, strontium carbonate, compounds thereof and combinations thereof. Supported metal catalysts can also have supporting materials made from one or more compounds. More preferred supports are carbon, titania and alumina. Further preferred supports are carbons with a surface area greater than 100 m ² /g. A further preferred support is carbon with a surface area greater than 200 m ² /g. Preferably, the carbon has an ash content that is less than 5% by weight of the catalyst support; the ash content is the inorganic residue (expressed as a percentage of the original weight of the carbon) which remains after incineration of the carbon. The preferred content of the metal catalyst in the supported catalyst is from about 0.1% to about 20% of the supported catalyst based on metal catalyst weight plus the support weight. A more preferred metal catalyst content range is from about 1% to about 10% of the supported catalyst.

Combinations of metal catalyst and support system may include any one of the metals referred to herein with any of the supports referred to herein. Preferred combinations of metal catalyst and support include palladium on carbon, palladium on calcium carbonate, palladium on barium sulfate, palladium on alumina, palladium on titania, platinum on carbon, platinum on alumina, platinum on silica, iridium on silica, iridium on carbon, iridium on alumina, rhodium on carbon, rhodium on silica, rhodium on alumina, nickel on carbon, nickel on alumina, nickel on silica, rhenium on carbon, rhenium on silica, rhenium on alumina, ruthenium on carbon, ruthenium on alumina and ruthenium on silica.

Further preferred combinations of metal catalyst and support include palladium on carbon, palladium on alumina, palladium on titania, platinum on carbon, platinum on alumina, rhodium on carbon, rhodium on alumina, ruthenium on carbon and ruthenium on alumina.

The method of the invention will now be described with reference to FIG. 1 to FlG. 3. Referring now to FlG. 1, a process flow diagram of an embodiment of the method 10 of the invention is shown. In the method 10, starting material composition 12 is provided that comprises a δ9 unsaturated fatty acid, a δ9 unsaturated fatty ester, a salt thereof, or a mixture thereof. In reaction 14, starting material composition 12 is cross-metathesized with a short-chain internal olefin 16

in the presence of a first metathesis catalyst 17 to produce cross-metathesis products 18 comprising (i) one or more olefins 20, and (ii) one or more acid-, ester-, or salt- functionalized alkenes 22. Following this, at least a portion of the acid-, ester-, or salt-functional ized alkene 22 is separated 23 from the remaining cross-metathesis products 18. Spent metathesis catalyst 17 may also be removed. In the next step, the isolated acid-, ester-, or salt-functionalized alkene 22 is then self-metathesized 24 in the presence of a second metathesis catalyst 28 to produce a Cl 8 diacid, diester, or disalt alkene 30 and one or more olefin products 32. Optionally, the Cl 8 diacid, diester, or disalt alkene can be hydrogenated to form a saturated C 18 diacid, diester, or disalt compound.

If the starting material comprises a fatty ester in glyceride form, the glyceride may be converted (e.g., by transesterification) into free fatty esters prior to being cross-metathesized with the short-chain internal olefin, or the glyceride can be cross- metathesized with the short-chain internal olefin followed by conversion (e.g., by transesterification) into free fatty esters.

Referring now to FIG. 2, a process flow diagram of an embodiment of the method 100 of the invention is shown. In this embodiment, a fatty acid triglyceride starting material is converted into free fatty esters prior to cross-metathesizing the free fatty esters with a short-chain internal olefin. In a first step of the method, triglyceride 102 and alcohol 104 are trans-esterified 106 in the presence of transesterification catalyst 105. Trans-esterification reaction 106 converts triglyceride 102 into glycerol 108 and free fatty esters 1 10. Together, the glycerol 108 and free fatty acid esters 1 10 are referred to as trans-esterification products 1 15. After transesterification reaction 106, a separation 1 14 (e.g., water wash or distillation) is conducted on the trans-esterification products 1 15 in order to separate the glycerol 108 from the free fatty acid esters 1 10. Spent metathesis catalyst 105 may also be removed.

After separation, a cross-metathesis reaction 1 18 is conducted between the free fatty esters 1 10 and short-chain internal olefin 1 16. The cross-metathesis 1 18 is conducted in the presence of a metathesis catalyst 120 in order to form cross- metathesis products 122 comprising one or more olefins 124 and one or more ester- functionalized alkenes 126. Following this, at least a portion of the ester-

functionalized alkenes 126 are separated 128 (e.g., using distillation) from the cross- metathesis products 122. The isolated ester-functionalized alkene 126 is then self- metathesized 129 in the presence of a second metathesis catalyst 130 to produce the self-metathesis products 132 comprising a diester alkene 134 and one or more olefin products 136.

Referring to FIG. 3, a process flow diagram of another embodiment of the method 200 of the invention is shown. In this embodiment, a fatty acid triglyceride starting material is cross-metathesized with a short-chain internal olefin. In the first reaction of method 200, triglyceride 202 and short-chain internal olefin 216 are cross-metathesized 218 in the presence of a metathesis catalyst 220 to form cross- metathesis products 222. Cross-metathesis products 222 comprise one or more olefins 224 and one or more ester-functionalized alkenes 225. In this embodiment, the ester-functionalized alkenes 225 are triglycerides. The cross-metathesis products 222 are then separated 228 into one or more ester-functionalized alkenes (triglyceride) products 225 and one or more olefins 224. Spent metathesis catalyst 220 can also be removed. Following this, the ester-functionalized alkene (triglyceride) products 225 are trans-esterified 206 with an alcohol 204 in the presence of a trans-esterification catalyst 205. Trans-esterification reaction 206 converts the ester-functionalized alkene (triglyceride) products 225 into trans- esterification products 215 comprising glycerol 208 and free ester-functionalized alkene 240. After trans-esterification reaction 206, a separation 214 is conducted in order to separate the glycerol 208 from the free ester-functionalized alkene 240. The free ester-functionalized alkene 240 is then self-metathesized 228 in the presence of a metathesis catalyst 230 in order to form a diester alkene product 234 and one or more olefin products 236. In an alternative embodiment (not shown in FIG. 3), the ester-functionalized alkene (triglyceride) is self-metathesized and the resulting product is trans-esterified to produce glycerol and free ester-functionalized alkene.

In an exemplary embodiment, as shown in FIG. 2 A, triglyceride 102A is reacted with methanol 104A in trans-esterification reaction 106A in the presence of trans-esterification catalyst 105A. Trans-esterification reaction 106A converts triglyceride 102A into glycerol 108A and free fatty acid methyl esters HOA. Collectively, glycerol 108A and free fatty acid methyl esters 1 1OA are referred to as

trans-esterification products 1 15A. In this embodiment, the free fatty acid methyl esters 1 1OA comprise methyl oleate (i.e., the methyl ester of oleic acid), methyl linoleate (i.e., the methyl ester of linoleic acid), and methyl linolenate (i.e., the methyl ester of linolenic acid). After trans-esterification reaction 106A, separation process 1 14A is conducted on the trans-esterification products 1 15A in order to separate the glycerol 108A from the free fatty acid methyl esters 1 1OA. Spent metathesis catalyst 105A can also be removed. Following separation, the free fatty acid methyl esters 1 1OA and 2-butene 1 16A (i.e., a short-chain internal olefin) are cross-metathesized 1 18A in the presence of a metathesis catalyst 120A to form cross-metathesis products 122A comprising olefins 124A and ester- functional ized alkenes 126A. The cross-metathesis products 122A are then separated by separation process 128A into product streams comprising 9-undecenoic acid methyl ester 125 A, 2-undecene 127 A, 2-octene 129 A, 2, 5-heptadiene 13 IA, and 2-pentene 133A. Next, 9-undecenoic acid methyl ester 125 A is self-metathesized 140A in the presence of a metathesis catalyst 142A to form self-metathesis products 143A comprising a Cl 8 diester alkene 144A and 2-butene 146A. Optionally, the Cl 8 diester alkene 144A can be hydrogenated to form a saturated Cl 8 diester 148A.

In another exemplary embodiment, as shown in FIG. 2B, triglyceride 102B is reacted with methanol 104B in trans-esterification reaction 106B in the presence of trans-esterification catalyst 105B. Trans-esterification reaction 106B converts triglyceride 102B into trans-esterification products 1 15B including glycerol 108B and free fatty acid methyl ester HOB. After trans-esterification reaction 106B, separation process 1 14B is conducted on the trans-esterification products 1 15B in order to separate the glycerol 108B from the free fatty acid methyl ester 1 1OB. Spent metathesis catalyst 105B can also be removed. Following separation, fatty acid methyl ester HOB and 3-hexene 1 16B (i.e., a short-chain internal olefin) are cross-metathesized 1 18B in the presence of a metathesis catalyst 120B to form cross-metathesis products 122B comprising olefins 124B and ester-functionalized alkenes 126B. Cross-metathesis products 122B are separated via separation process 128B into product streams comprising: 9-dodecenoic acid methyl ester 125 B, 3- dodecene 127B, 3-nonene 129B, 3, 6-nonadiene 13 IB, and 3-hexene 133B. Next, 9- dodecenoic acid methyl ester 125 B is self-metathesized 140B in the presence of a

metathesis catalyst 142B to form self-metathesis products 143 B comprising a Cl 8 dimethyl ester alkene 144B and 3-hexene 146B. Optionally, the C 18 diester alkene can be hydrogenated to form a saturated Cl 8 dimethyl ester 148B.

The invention will now be described with reference to the following non- limiting examples.

EXAMPLES

EXAMPLE 1 : Synthesis of 1, 18-Diester (1,18-dimethyl ester of 9-octadecene) from 3-Hexene and Soybean Oil

O O O

Sov _b eaπ Oil or Metathesis Catalyst ji Metathesis Catalyst JL . . _^ J

NMM sSiate ^{and 3'hexen} t ^KO ^fT^ ^hi g ^h vacuum * ^MeO ^^p^ ^OMe

R = glyceride or methyl « , 1, 18-Diester of 9-Octadecene

- O-πθXθπθ

Step 1 : Production of Methyl 9-dodecenoate [CH ₃ CH ₂ CH=CH(CH ₂ ^CO ₂ CH ₃ ]

Metathesis reactions were conducted in a 250 ml 3-neck round bottom Schlenk flask that was equipped with a reflux condenser (connected to a bubbler), two septa, a stir bar, and a thermocouple. Prior to adding any reactants, the apparatus was degassed with argon for thirty minutes. Then, 70 ml (64.4 g) of degassed soybean oil (Cargill soybean oil (Salad oil), Lot # F4102) was added to the apparatus. In a separate container, 3-hexene was degassed with argon for one hour. Following degassing, 127 ml (86.4 grams) of the degassed 3-hexene was added to the flask using a graduated cylinder. The resulting mixture was degassed for fifteen minutes with argon. The mixture was then heated to 65 ⁰ C before adding the metathesis catalyst.

Metathesis catalyst (C827, Lot # 067-050B) was added to the degassed mixture of soybean oil and 3-hexene in the amount shown in TABLE 1. In each case, the resulting mixture was allowed to react at 65 ⁰ C, with aliquots taken at 2, 4, and 6 hours to check for conversion using a gas chromatograph. Maximum conversion was reached after two hours in all cases. In each case, after reacting for 6 hours, 1.30 grams of activated clay (Pure-Flo B80 natural Bleaching Adsorbent) was added, and the resulting composition was stirred overnight. Following this, the composition was filtered through a bed of silica to remove the activated clay and metathesis catalyst. The filtrates were sealed in a sample bottle and refrigerated.

Percent yield of methyl 9-dodecenoate was determined using a gas chromatograph. The resulting data is presented in TABLE 1.

TABLE

Catalyst 827 loading in ppm per double bond of SBO. 3-Hexene was added in 3 equivalents per double bond of SBO.

GC yield after 2 hours, yields did not change significantly at 6 hours.

Step 2: Self-Metathesis of Methyl 9-Dodecenoate Samples of methyl 9-dodecenoate were warmed to temperature (see, TABLE

2) and were degassed with argon for 30 minutes. Next, a metathesis catalyst (see, TABLE 2) was added to the methyl 9-dodecenoate and vacuum was applied to provide a pressure of <1 mmHg. The methyl 9-dodecenoate was then allowed to self-metathesize for the time reported in TABLE 2. GC analysis indicated that 1, 18- dimethyl ester of 9-octadecene [CH ₃ O ₂ C(CH ₂ ) ₇ CH=CH(CH ₂ ) ₇ CO ₂ CH ₃ ] was produced in the yield reported in TABLE 2.

TABLE 2

EXAMPLE 2: Vacuum Distillation of 9C ₁₂ OzMe.

A glass 2.0 L 3-necked round bottom flask with a magnetic stirrer, packed column, distillation head, and temperature controller was charged with esterified products and was placed in a heating mantle. The flask was attached to a 2-inch x 36-inch glass distillation packed column containing 0.16" Pro-Pak™ stainless steel saddles. The distillation column was connected to a fractional distillation head, which was connected to a vacuum line. A 500 mL pre-weighed round bottom flask was used to collect the distilled fractions. During distillation, vacuum was applied to provide a pressure of <1 mmHg. TABLE 3 contains the vacuum distillation results.

TABLE 3: Distillation Data

6C ₁₅ + 6,9C ₁₅ impurities were separated from 9Ci ₂ O ₂ Me by equilibrating the distillation column for 24 hours, followed by collecting 6C ₁₅ + 6,9Ci ₅ with a reflux ratio of 1 : 10 (i.e. 1 drop collected for every 10 drops sent back to the packed column). This procedure demonstrates that 9C ₁₂ O ₂ Me (275.4 g.) could be isolated in 50.9% yield and in 99.2% chemical purity. The 6Ci ₅ + 6,9Ci ₅ impurities could be removed by fractional distillation. EXAMPLE 3: Self-metathesis of methyl 9-decenoate.

Methyl 9-decenoate (25g, 1 14 mmol, -90% chemical purity) obtained by ethenolysis of methyl oleate was charged in a 250 mL round-bottomed flask and was degassed with argon for 30 min. C823 metathesis catalyst (127 mg, 0.15 mmol, 0.13 mol %) was then added, and the reaction contents were heated to 35 ⁰ C under vacuum for 16 hrs. A 1.0 M solution of tris(hydroxymethyl)phosphine (4 mL) was then added and the reaction contents were heated to 90 ⁰ C for 4 hr. The reaction contents were then cooled to room temperature and were diluted with 50 mL of ethyl acetate. The diluted reaction contents were then washed sequentially with (1) 50 mL of 1.0 M aqueous HCl, (2) water, and (3) brine. The resulting organic phase was then dried with anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation. 1 gram of the crude diester (1,18-dimethyl 9-octadecenedioate) was then dissolved in 4.5 mL of hexanes and the resulting homogeneous solution was cooled to -1 1 ⁰ C for 5 hrs. The crystals that formed were filtered and air-dried. GC analysis of the crystals indicated 95.8% chemical purity and 99: 1 E:Z isomeric ratio.

EXAMPLE 4: Preparation of 1.12-Diester of Dodecene from Methyl-9-

Dodecenoate and Methyl-3-Pentenoate.

Step 1 : Methyl-9-Dodecenoate was prepared as described in Step 1 of EXAMPLE

1. Step 2: Cross-metathesis of Methyl 9-dodecenoate with Methyl-3-Pentenoate

Methyl 9-dodecenoate and methyl-3-pentenoate were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 4). Next, a metathesis catalyst (see, TABLE 4) was added to the methyl 9-dodecenoate and methyl-3-pentenoate mixture. The mixture was then allowed to metathesize for the time reported in TABLE 4. GC analysis indicated that 1,12-dimethyl ester of dodecene [CH ₃ O ₂ C(CH ₂ ) ₇ CH=CH(CH ₂ )CO ₂ CH ₃ ] was produced in the GC yield reported in TABLE 4.

9C ₁₂ -O ₂ Me 3-penteπoate

TABLE 4

* ND = no data

¹ No conversion was seen at lower catalyst loadings

EXAMPLE 5: Preparation of Methyl 1 1 -Chloro-9-undecenoate from Methyl-9-

Dodecenoate and 1 ,4-Dichloro-2-butene.

Step 1 : Methyl-9-Dodecenoate was prepared as described in Step 1 of EXAMPLE

1.

Step 2: Cross-metathesis ofmethyl-9-dodecenoate with l,4-dichloro-2-butene

Methyl 9-dodecenoate and l,4-dichloro-2-butene were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 5). Next, a metathesis catalyst (see, TABLE 5) was added to the methyl 9-dodecenoate and l,4-dichloro-2-butene mixture. The mixture was then allowed to metathesize for the time reported in TABLE 5. GC analysis indicated that the product [CH ₃ O ₂ C(CH ₂ ) ₇ CH=CHCH ₂ C1] was produced in the GC yield reported in TABLE 5.

9C ₁₂ -O ₂ Me 1 ,4-dιchloro-2-butene 9C ₁₈ -(O ₂ Me) ₂

TABLE 5

^* ND = no data

¹ 827 was initiated at 60°C, then reaction removed from heat to stir at room temp Freshly distilled 1 ,4- dιchloro-2-butene was used ² 1 ,4-dιchloro-2-butene used directly from bottle with no distillation

EXAMPLE 6: Preparation of Methyl 12-Acetoxy-9-Dodecenoate from Methyl-9- dodecenoate and 3-Buten-l-yl Acetate.

Step 1 : Methyl 9-dodecenoate was prepared as described in Step 1 of EXAMPLE 1. Step 2: Cross-Metathesis of methyl 9-dodecenoate with 3-buten-l-yl acetate.

Methyl 9-dodecenoate and 3-buten-l-yl acetate were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 6). Next, a metathesis catalyst (see, TABLE 6) was added to the methyl 9-dodecenoate and 3- buten-1-yl acetate mixture. The mixture was then allowed to metathesize for the

time reported in TABLE 6. GC analysis indicated that the product [CH ₃ O ₂ C(CH ₂ ) ₇ CH=CH(CH ₂ ) ₂ CO ₂ CH ₃ ] was produced in the GC yield reported in TABLE 6.

9C ₁₂ -O ₂ Me

TABLE 6

827 was initiated at 6O ⁰ C, then reaction removed from heat to stir at room temp

EXAMPLE 7: Preparation of Methyl 12-Trimethylsiloxy-9-Dodecenoate from

Methyl 9-Dodecenoate and 3-Buten-l-yl trimethylsilyl ether.

Step 1 : Methyl 9-dodecenoate was prepared as described in Step 1 of EXAMPLE 1.

Step 2: Cross-Metathesis of Methyl 9-dodecenoate with 3-buten-l-yl trimethylsilyl ether.

Methyl 9-dodecenoate and 3-buten-l -yl trimethylsilyl ether were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 7). Next, a metathesis catalyst (see, TABLE 7) was added to the methyl 9- dodecenoate and 3-buten-l-yl trimethylsilyl ether mixture. The mixture was then allowed to metathesize for the time reported in TABLE 7. GC analysis indicated that the product [CH ₃ O ₂ C(CH ₂ ) ₇ CH=CH(CH ₂ ) ₂ OSi(CH ₃ ) ₃ ] was produced in the GC yield reported in TABLE 7.

TABLE 7

827 was initiated at 60°C, then reaction removed from heat to stir at room temp

EXAMPLE 8: Preparation of Methyl 12-bromo-9-Dodecenoate from Methyl-9- dodecenoate and l-bromo-3-hexene.

Step 1 : Methyl 9-dodecenoate was prepared as described in Step 1 of EXAMPLE 1. Step 2: Cross-Metathesis of Methyl 9-dodecenoate with l-bromo-3-hexene.

Methyl 9-dodecenoate and l-bromo-3-hexene were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 8). Next, a metathesis catalyst (see, TABLE 8) was added to the methyl 9-dodecenoate and 1- bromo-3-hexene mixture. The mixture was then allowed to metathesize for the time reported in TABLE 8. GC analysis indicated that the product [CH ₃ O ₂ C(CH ₂ ) ₇ CH=CH(CH ₂ ) ₂ Br] was produced in the GC yield reported in TABLE 8.

9C ₁₂ -O ₂ Me 9C ₁₈ -(O ₂ Me) ₂

TABLE 8

EXAMPLE 9: Preparation of Methyl 1 l -chloro-9-undecenoate from Methyl-9- dodecenoate and allyl chloride.

Step 1 : Methyl 9-dodecenoate was prepared as described in Step 1 of EXAMPLE 1.

Step 2: Cross-Metathesis of methyl 9-dodecenoate with Allyl chloride. Methyl 9-dodecenoate and allyl chloride were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 9). Next, a metathesis catalyst (see, TABLE 9) was added to the methyl 9-dodecenoate and allyl chloride mixture. The mixture was then allowed to metathesize for the time reported in TABLE 9. GC analysis indicated that the product [CH ₃ O ₂ C(CH ₂ ) ₇ CH=CHCH ₂ C1] was produced in the GC yield reported in TABLE

9.

9C ₁₂ -O ₂ Me 9C ₁₈ -(O ₂ Me) ₂

TABLE 9

* Allyl chloride was freshly distilled.

EXAMPLE 10: Preparation of Methyl 12.12-Diethoxy-9-Dodecenoate from

Methyl-9-dodecenoate and 3-butenal diethyl acetal.

Step 1 : Methyl 9-dodecenoate was prepared as described in Step 1 of EXAMPLE 1.

Cross-Metathesis of methyl-9-dedecenoate with 3-butenal diethyl acetal.

Methyl 9-dodecenoate and 3-butenal diethyl acetal were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 10). Next, a metathesis catalyst (see, TABLE 10) was added to the methyl 9-dodecenoate and 3-butenal diethyl acetal mixture. The mixture was then allowed to metathesize for the time reported in TABLE 10. GC analysis indicated that the product

[CH ₃ O ₂ C(CH2) ₇ CH=CHCH ₂ CH(OCH ₂ CH ₃ ) ₂ ] was produced in the GC yield reported in TABLE 10.

9C ₁₈ -(O ₂ Me) ₂

TABLE 10

EXAMPLE 1 1 : Preparation of Methyl 12-tert-Butoxy-9-Dodecenoate from Methyl- 9-dodecenoate and l-tert-butoxybut-3-ene.

Step 1 : Methyl 9-dodecenoate was prepared as described in Step 1 of EXAMPLE 1. Step 2: Cross-Metathesis of methyl-9-dodecenoate with l-tert-butoxybut-3-ene. Methyl 9-dodecenoate and l-tert-butoxybut-3-ene were combined and degassed with argon for 30 minutes, then warmed to temperature (see, TABLE 1 1). Next, a metathesis catalyst (see, TABLE 1 1) was added to the methyl 9-dodecenoate and l-tert-butoxybut-3-ene mixture. The mixture was then allowed to metathesize for the time reported in TABLE 1 1. GC analysis indicated that the product [CH ₃ O ₂ C(CH ₂ ) ₇ CH=CH(CH ₂ ) ₂ OC(CH ₃ ) ₃ ] was produced in the GC yield reported in TABLE I l .

9C ₁₂ -O ₂ Me

TABLE 1 1

Other embodiments of this invention will be apparent to those skilled in the art upon consideration of this specification or from practice of the invention disclosed herein. Various omissions, modifications, and changes to the principles and embodiments described herein may be made by one skilled in the art without departing from the true scope and spirit of the invention which is indicated by the following claims. All patents, patent documents, and publications cited herein are hereby incorporated by reference as if individually incorporated.