PROCESS FOR SYNTHESIS OF !NDENES

INTRODUCTION

[0001] The present invention relates to a process for the synthesis of 2,3,4,5,6,7- substituted indenes, which are useful precursors for the formation of certain ansa- metallocene catalysts.

BACKGROUND OF THE INVENTION

[0002] It is well known that ethylene (and a-olefins in general) can be readily polymerized at low or medium pressures in the presence of certain transition metal catalysts. These catalysts are generally known as Ziegler-Natta type catalysts.

[0003] A particular group of these Ziegler-Natta type catalysts, which catalyse the polymerization of ethylene (and a-olefins in general), comprise an aluminoxane activator and a metallocene transition metal catalyst, fvletailocenes comprise a metal bound between two r -cyclopentadienyl type ligands. Generally the n _, ⁵ -cyclopentadienyl type ligands are selected from r -cyclopentadienyi, r -indeny! and r -fluorenyl.

[0004] It is also well known that these r -cyclopentadienyl type ligands can be modified in a myriad of ways. One particular modification involves the introduction of a linking group between the two cyclopentadienyl rings to form ansa-metallocenes.

[0005] WO201 1/051705 describes certain ansa-metailocene catalysts that demonstrate particularly high catalytic performance when utilised for the polymerization of polyethylene. The catalysts described in WO201 1/051705 comprise a metal atom bound between two inter-linked indenyl moieties. The indeny! moieties bear substituents in the 2,3,4,5,6 and 7-positions of each indenyl moiety, and a linking group (such as -CH2-CH2-) connects the 1 -positions of the respective indenyl moieties together.

[0006] In the synthesis of such ansa-metallocene catalysts, the desired 2,3,4,5,6,7- substituted indene precursor is initially formed and then the two indenyl moieties are cross-linked by the insertion of the linking group that connects the 1 -positions of two indenyl moieties together. The resultant linked bis(2,3,4,5,6,7-substituted indenyl) ligand is then complexed with the desired metal to form the a/isa-metallocene catalyst.

[0007] As part of this synthetic procedure, there is a need for a simple, efficient and scalable process for the formation of the desired 2,3,4,5,6,7-substituted indene precursors, [0008] O'Hare et al. (Organometallics 1992, 11, 48) describes a process for the formation of a heptamethyiindene as a precursor for the formation of certain metaliocene catalysts [namely b!s(heptamethylindenyI)iron(II),

bis(heptamethylindenyl)-iron(lll) hexafluorophosphate,

bis(heptamethylindenyi)cobalt(lll) hexafluorophosphate and

bis(heptamethylindenyt)cobait(ll)].

[0009] The process described by O'Hare ef al involves a number of different reaction steps. The first step involves reacting tiglic acid with thionyl chloride under reflux for 5 hours. Excess thionyl chloride was evaporated off at 78 °C. The product was then distilled under reduced pressure (10 mmHg, ca. 37 ^D C) to give a colourless liquid (tigloyf chloride) in a 95% yield. In a subsequent step, a mixture of AICI ₃ is stirred in CS ₂ at -5 °C and a mixture of 1 ,2,3,4- tetramethylbenzene and tigloyl chloride were added slowly over a period of 1 hour. After the addition, the mixture turned red-brown and solid CS ₂ was added. The mixture was warmed to room temperature and stirred overnight. It was then heated to 50 °C for 2 hours and then poured into a mixture of ice and concentrated HCI before extracting with diethyl ether and drying the ether layer over CaCfe. Upon distillation, a dark brown crude liquid was obtained, which was further distilled under reduced pressure giving a yellow oily liquid (2,3,4,5,6,7- hexamethlyindan-1 -one ketone) in 85% yield. In a further step, the ketone is reacted with LiMe to form heptamethyiindene.

[0010] While the process described above enables the desired indene products to be formed, there remains a need for improved methods of forming the particular 2,3,4,5,6,7-substituted indenes that can be used for the formation of ansa- metaiiocene catalysts, such as those described in WO201 1/05 705. In particular, there is a need for improved synthetic methods that are simple, efficient, provide good product purity and which are suitable for scale-up.

SUMMARY OF THE INVENTION

[0011] According to a first aspect of the present invention there is provided a process for the preparation of a compound of the formula I shown below:

(I)

wherein R ₁ and R ₂ are each (1-10C)alkyl;

and wherein the process comprises the steps of:

(i) reacting a compound of formula A:

(A)

wherein and R ₂ are each as defined above;

with a chlorinating or brominating agent to form a compound of formula B:

(B)

wherein R-i and R ₂ are each as defined above and X is chloro or bromo; and then adding 1 ,2,3,4-tetramethylbenzene and a Lewis acid catalyst to the reaction mixture to react with compound B to form a compound of formula C:

(C) wherein Ri and R ₂ are each as defined above;

(ii) reacting the compound of formula C with a solution of a hydride transfer reagent to reduce the ketone to the corresponding alcohol and then by adding a dehydrating agent to the reaction mixture to form a compound of formula I, namely dehydrating the alcohol.

[0012] Step (i) of the process defined above is a "one-pot" step. Thus, when it is stated in step (i) that 1 ,2,3,4-tetramethylbenzene and a Lewis acid catalyst are added to the reaction mixture to react with compound B to form a compound of formula C, it is meant that the 1 ,2,3,4-tetramethylbenzene and a Lewis acid catalyst are added directly to the reaction mixture comprising the compound of formula B. It is not necessary to isolate the compound of formula B prior to the addition of 1 ,2,3,4-tetramethyibenzene and the Lewis acid catalyst.

[0013] Suitably, step (ii) is also a "one-pot" reaction in which the dehydration of the alcohol formed by the reduction of the ketone of formula C is facilitated by the addition of a dehydrating agent directly to the reaction mixture comprising the alcohol (the reduced ketone), it is not necessary to isolate the alcohol (the reduced ketone) prior to the addition of the dehydrating agent.

[0014] According to a second aspect of the present invention there is provided a process for the preparation of a compound of the formula C as defined above,

wherein the process comprise the steps of:

(i) reacting a compound of formula A:

(A)

wherein R-i and R ₂ are each as defined above;

with a chlorinating or brominating agent to form a compound of formula B:

(B)

wherein and R ₂ are each as defined above and X is chloro or bromo;

and then adding 1 ,2,3,4-tetramethylbenzene and a Lewis acid catalyst to the reaction mixture to react with compound B to form a compound of formula C:

(C)

wherein R ₁ and R ₂ are each as defined above.

[0015] According to a third aspect of the present invention there is provided a process of forming a compound of Formula I as defined herein, said process comprising reacting a compound of formula C as defined herein with a solution of a hydride transfer reagent to reduce the ketone to the corresponding alcohol and then dehydrating the alcohol to form a compound of Formula I as defined herein,

[0016] According to a fourth aspect of the present invention there is provided a process for forming a compound of formula II

(II)

wherein

R-j , R ₂ are as defined herein; and

L is a bridging group of the formula -[C(R R ^y )] _n - wherein n is 1 , 2 or 3 and R* and R ^¥ are each independently hydrogen, (1-6C)alkyl(2-6C)alkenyl, (2-6C)alkynyl or (1 -6C)alkoxy; or a group -SiR _a R _b wherein R _a and R _b are each independently selected from (1 -6C)alkyi, (2-6C)alkenyi, (2-6C)alkynyl, (1-6C)alkoxy or phenyl; the process comprises:

forming a compound of formula I by a process as defined herein;

reacting the compound of formu!a I with an organolithium, organosodium or organopotassium compound of the formula:

MQ

wherein M is lithium, sodium, or potassium and Q is an (1 -6C)alkyl or aryl group;

to form a compound of formula D shown below:

(D)

(iii) reacting two equivalents of a compound of formula D shown above with one equivalent of a compound having formula E shown below:

ZrL-Z ₂

(E) wherein L is as defined hereinbefore and Z and Z ₂ are suitable leaving groups (such as halo (e.g. chloro or bromo)) to form a compound of formula II .

[0017] According to a fifth aspect of the present invention there is provided a process for forming a compound of formula I II

wherein R ₂ and L are as defined herein;

X is zirconium, hafnium or titanium;

Y is selected from halo, hydride, a phosphonated or sulfonated anion, or a (1~6C)alkyl, (1 -6C)alkoxy, aryl or aryloxy group which is optionally substituted with halo, nitro, amino, phenyl, (1 -6C)alkoxy, or Si[(1 -4C)alkyl] ₃ .

wherein the process comprises:

(i) forming a compound of formula li by the process defined above in the fourth aspect of the present invention;

(ii) reacting the compound of formula II with a compound of the formula:

X(Y) ₂ (Z ₃ ) ₂

wherein X and Y are as defined above and Z ₃ is a suitable leaving group (e.g. chloro).

[0018] The present invention also relates to a compound of formula I, ! I or ill as defined herein obtainable by, obtained by, or directly obtained by any one of the processes defined herein.

[0019] Preferred embodiments are disclosed in the sub-claims.

DETAILED DESCRIPTION OF THE INVENTION

Definitions

Alky!

[0020] The term "alkyl" as used herein includes reference to straight or branched chain alkyl moieties, typically having 1 , 2, 3, 4, 5 or 6 carbon atoms. This term includes reference to groups such as methyl, ethyl, propyl (n-propy! or isopropyl), butyl (n-butyi, sec-butyl or tert-butyl), pentyi, hexyl and the like. In particular, an alkyl may have 1 , 2, 3 or 4 carbon atoms.

Alkenyi

[0021] The term "alkenyi" as used herein includes reference to straight or branched chain alkenyi moieties, typically having 1 , 2, 3, 4, 5 or 6 carbon atoms. The term includes reference to alkenyi moieties containing 1 , 2 or 3 carbon-carbon double bonds (C=C). This term includes reference to groups such as ethenyl (vinyl), propenyl (allyl), butenyl, pentenyl and hexenyl, as well as both the cis and trans isomers thereof.

Alkynyl [0022] The term "alkynyf as used herein includes reference to straight or branched chain alkynyl moieties, typically having 1 , 2, 3, 4, 5 or 6 carbon atoms. The term includes reference to alkynyS moieties containing 1 , 2 or 3 carbon-carbon triple bonds (C=C). This term includes reference to groups such as ethynyl, propynyl, butyny!, pentyny! and hexynyl.

Alkoxy

[0023] The term "aikoxy" as used herein includes reference to -O-alkyl, wherein alkyl is straight or branched chain and comprises 1 , 2, 3, 4, 5 or 6 carbon atoms. In one class of embodiments, alkoxy has 1 , 2, 3 or 4 carbon atoms. This term includes reference to groups such as methoxy, ethoxy, propoxy, isopropoxy, butoxy, tert-butoxy, pentoxy, hexoxy and the like.

Aryl

[0024] The term "aryi" as used herein includes reference to an aromatic ring system comprising 6, 7, 8, 9 or 10 ring carbon atoms. Aryl is often phenyl but may be a polycyclic ring system, having two or more rings, at least one of which is aromatic. This term includes reference to groups such as phenyl, naphthyl and the like.

Halogen

[0025] The term "halogen" or "halo" as used herein includes reference to F, CI, Br or I. In a particular, halogen may be F or Ci, of which CI is more common.

Substituted

[0026] The term "substituted" as used herein in reference to a moiety means that one or more, especially up to 5, more especially 1 , 2 or 3, of the hydrogen atoms in said moiety are replaced independently of each other by the corresponding number of the described substituents. The term "optionally substituted" as used herein means substituted or unsubstituted.

[0027] It will, of course, be understood that substituents are only at positions where they are chemically possible, the person skilled in the art being able to decide (either experimentally or theoretically) without inappropriate effort whether a particular substitution is possible. For example, amino or hydroxy groups with free hydrogen may be unstable if bound to carbon atoms with unsaturated (e.g. olefinic) bonds. Additionally, it will of course be understood that the substituents described herein may themselves be substituted by any substituent, subject to the aforementioned restriction to appropriate substitutions as recognised by the skilled person. Compounds of formula I, II and III

[0028] As indicated above, the present invention relates to preparation of compounds of formula !, II and ill by the processes defined herein.

[0029] In the compounds of formula I, I! and III defined herein, and R ₂ are each independently selected from (1 -10C)alkyl. Suitably, R and R ₂ are each independently selected from (1 -3C)alkyf. In an embodiment, and R ₂ are each independently selected from (1-2C)alkyl. In a particular embodiment, and R ₂ are both methyl.

[0030] Suitably, R _a and R _b are each independently selected from (1 -4C)alkyl, (2- 4C)alkenyl or (2-4C)alkynyl. Even more suitably, R _a and R _b are each independently selected from methyl, propyl and allyl. Most suitably, R _a and R _b are both methyl.

[0031] In an embodiment, L is -CH ₂ -CH ₂ -, -CH ₂ -CH ₂ -CH ₂ - or a group -SiR _a R _b wherein R _a and R _b are each independently selected from methyl, propyl and allyl.

[0032] In an embodiment, L is -CH ₂ -CH ₂ -, -CH ₂ -CH ₂ -CH ₂ - or a group -SiR _a R _b wherein R _a and R _b are each independently selected from methyl and allyl.

[0033] In an embodiment, L is -CH ₂ -CH ₂ -, -CH ₂ -CH ₂ -CH ₂ - or a group -SiMe ₂ or - Si(Me)(ai!yl).

[0034] In a particular embodiment, L is -CH ₂ -CH ₂ - or a group -Si e ₂ or -Si(Me)(allyl).

[0035] In a particular embodiment, L is -CH ₂ -CH ₂ - or -SiMe ₂ .

[0036] In an embodiment, X is zirconium or hafnium.

[0037] In a particular embodiment, X is zirconium.

[0038] In a particular embodiment, X is hafnium.

[0039] In an embodiment, each Y group is the same.

[0040] In an embodiment, Y is selected from halo, (1 -6C)atkyl or phenyl, wherein the alkyl or phenyl group is optionally substituted with halo, nitro, amino, phenyl, (1- 6C)alkoxy, or Si[(1 -4C)alkyt] ₃ .

[0041] In an embodiment, Y is selected from halo or a (1-6C)alkyl group which is optionally substituted with halo, nitro, amino, phenyl, (1 -6C)alkoxy, or Si[(1-4C)alkyl] ₃ .

[0042] In another embodiment, Y is selected from halo or a (1-6C)aIkyl group which is optionally substituted with halo, phenyl, or Si[(1 -2C)alkyl] ₃ .

[0043] In another embodiment, Y is selected from chloro, bromo, or a (1 -4C)alky! group which is optionally substituted with halo, phenyl, or Si[Me] ₃ . [0044] In a particular embodiment, Y is selected from chloro or a (1-4C)alkyl group which is optionally substituted with phenyi or Si[Me] ₃ .

[0045] In a further embodiment, Y is chloro, bromo or methyl.

[0046] In a further embodiment, Y is ch!oro or bromo.

[0047] In a further embodiment, Y is chloro.

[0048] In another embodiment, Y is methyl.

[0049] In a particular embodiment, R-i and R ₂ are both methyl; L is -CH ₂ -CH ₂ -, -CH ₂ - CH ₂ -CH ₂ - or a group -SiR _a R _b wherein R _a and R _b are each independently selected from methyl, propyl and ally!; X is zirconium or hafnium; and Y is selected from ch!oro, bromo, or a (1-4C)alkyl group which is optionally substituted with halo, phenyl or Si[Me] ₃ .

[0050] !n a particular embodiment, and R ₂ are both methyl; L is -CH ₂ -CH ₂ -, -CH ₂ - CH ₂ -CH ₂ - or a group -SiR _a R _b wherein R _a and R _b are each independently selected from methyl and allyi; X is zirconium or hafnium; and Y is selected from chloro, bromo, or a (1- 4C)a1kyS group,

Process for producing compounds of formula I

[0051] As described hereinbefore, the present invention provides a process for the preparation of a compound of the formula I shown below;

(I)

comprising the steps (i) and (ii) defined above.

[0052] The process of the present invention provides a number of distinct advantages. Firstly, steps (i) and (ii) of the process defined herein for the first aspect of the present invention are both discrete "one-pot" steps. This provides a more facile process when compared to the synthetic approaches described in the prior art. It also provides some further advantages. [0053] For example, when compared with the process described by O'Hare ef al. (Organometallics 1992, 11, 48), step (i) of the process of the present invention has the advantages of:

• The reaction times and temperatures can be reduced, thereby making the reaction more cost effective and more suitable for scaie-up.

» The need for disti!lation is negated, which is time consuming and energy intensive

* The process can use different chlorinating agents (such as, for example, oxalyt chloride) to the SOCI ₂ used in the O'Hare et al. method which can be hazardous because it causes severe burns.

β The use of CS ₂ can also be avoided, which is flammable, toxic and has a very low flash point.

* The reaction can be carried out at room temperature, if so desired.

• The process of the present invention also enables the ketone (i.e. the compound of formula C) to be produced with high yield and with improved purity (in the example described herein, hexamethylindanone (lnd =0) is obtained with 96% yield).

[0054] in addition, the overall yield of the process is high (94% in the example provided herein) and the purity of the product is also high.

[0055] In step (ii), the use of a solution of a hydride transfer agent has been found to reduce the reaction time for the reduction of the ketone. Furthermore, the time required for the dehydration of the reduced ketone to form the compound of formula I is also reduced by the "one-pot" step (ii) reaction employed in the process of the present invention.

[0056] The first step [step (i)] of the reaction involves reacting a compound of formula A:

(A)

wherein Ri and R ₂ are each as defined herein;

with a chlorinating or brominating agent to form a compound of formula B:

(B)

wherein R and R ₂ are each as defined herein and X is chloro or bromo;

and then adding 1 ,2,3,4-tetramethyibenzene and a Lewis acid catalyst to the reaction mixture to react with compound B to form a compound of formula C:

(C)

[0057] This whole step is carried out as a "one-pot" reaction with the initial reaction to form compound B followed by the addition of the required reagents ( ,2,3,4- tetramethyibenzene and a Lewis acid catalyst) to subsequently form compound C,

[0058] The reactions that make up step (i) may be carried out in any suitable solvent. A person skilled in the art will know how to select suitable solvents for this reaction. Nontoxic polar solvents such as dichloromethane, THF, ethers (e.g. methyl t-butyl ether ( tBE) or dioxane) etc. are examples of solvents that can be used. In a particular embodiment, the solvent is dichloromethane.

[0059] A person skilled in the art will be able to select suitable reaction conditions {reaction atmosphere, reaction temperature, duration of the reaction and workup procedures) for this reaction.

[0060] Suitably, the process of step (i) may be carried out at room temperature (e.g. 20- 25 °C) or the reaction mixture may be heated, for example, up to a temperature of up to 80 °C depending on the solvent that is used.

[0061] The duration of step (i) is suitably between 1 and 24 hours, with reaction times of 16 hours or less being generally preferred.

[0062] Suitably, step (i) is carried out under an inert atmosphere, such as, for example, a nitrogen atmosphere. [0063] Any suitable chlorinating or brominating agent may be used for the reaction with the compound of formula A. Suitably, the chlorinating agent is selected from the group consisting of oxalyl chloride, PCl ₃ , PC! ₅ and SOCL ₂ and the brominating agent is selected from the group consisting of PBr ₃ and PBr ₅ .

[0064] In an embodiment, a chlorinating agent is used to form compounds of formula B in which X is chloro. In a further embodiment, a chlorinating agent selected from oxalyl chloride, PCI ₃ and/or PCI ₅ . In a particular embodiment, oxaly! chloride is used as the chlorinating agent.

[0065] The reaction between the compound of formula A and the chlorinating agent may take from 1 to 20 hours. Suitably, the reaction takes place at room temperature for up to 15 hours or, more preferably, up to 12 hours.

[0066] Following the reaction between the compound of formula A and the chlorinating or brominating agent to form a compound of formula B, a Lewis acid catalyst is added to the reaction mixture along with 1 ,2,3,4-tetramethylbenzene.

[0067] Any suitable Lewis acid catalyst may be used. In an embodiment, the Lewis acid catalyst is selected from AICI _3i AlBr ₃ and BCI ₃ . in a particular embodiment, the Lewis acid catalyst is A!CI ₃ ,

[0068] Suitably, the Lewis acid catalyst is added to the reaction mixture prior to the 1 ,2,3,4-tetramethylbenzene. The reaction mixture may be cooled, for example to less than 10°C, prior to the addition of the Lewis acid catalyst.

[0069] The reaction between the compound of formula B and the 1 ,2,3,4- tetramethylbenzene is allowed to proceed for up to 6 hours, and more preferabiy up to 4 hours.

[0070] The reaction may be quenched by the addition of an acid, for example concentrated hydrochloric acid, and optionally cooling the reaction mixture, for example by the addition of ice.

[0071] The product, namely the compound of formula C is then extracted from the reaction mixture using standard techniques.

[0072] In step (ii) of this process, the compound of formula C is reacted with a solution of a hydride transfer reagent to reduce the ketone to the corresponding alcohol, which is then dehydrated to form a compound of Formula I as defined herein. [0073] Again, this reaction can be carried out as a "one-pot" reaction. The first part of this reaction step involves the reduction of the compound of formula C. This provides a compound of the formula CR:

(CR)

This reduction is achieved by using a solution of a hydride transfer reagent. Suitable examples of hydride transfer reagents include LiAIH ₄ and NaBH ₄ . In a particular embodiment, the hydride transfer reagent is a solution of UAiH ₄ in a suitable solvent, such as, for example, THF.

[0074] This reaction is suitably carried out in an inert atmosphere, for example a nitrogen atmosphere. The reduction reaction suitably proceeds for up to 6 hours, and more preferably for up to 4 hours.

[0075] The reaction may proceed at any suitable temperature. For example, temperatures within the range of 0 to 30 °C may be used. Suitably, the solution of the hydride transfer reagent is cooied, for example to less than 10 °C, prior to the addition of the compound of formula C.

[0076] The reduction reaction is suitably quenched, for example by the addition of water. The reduced compound of formu!a C (compound CR) is then dehydrated by the addition of a dehydrating agent. Any suitable dehydrating agent may be used. Suitably, the dehydrating agent is an acid, for example concentrated sulphuric, hydrochloric or phosphoric acid. The direct addition of the dehydrating agent to the reaction mixture efficiently dehydrates the reduced form of the compound of formula C (compound CR) to provide the desired compound of formula I.

[0077] The reaction time for the dehydration step is typically up to 60 minutes, and more preferably up to 30 minutes.

[0078] The desired compound of formula I is then extracted using standard techniques. Process for producing compounds of formula II

[0079] According to a fourth aspect of the present invention there is provided a process for forming a compound of formula ll

(ii)

wherein

R _{1 t} R ₂ and L are as defined herein.

[0080] The process involves:

(i) forming a compound of formula i by a process as defined herein;

(ii) reacting the compound of formula I with an organolithium, organosodium or organopotassium compound of the formula:

MQ

wherein M is lithium, sodium, or potassium and Q is an (1-6C)alkyl or aryl group;

to form a compound of formula D shown below:

(iii) reacting two equivalents of a compound of formula D shown above with one equivalent of a compound having formula E shown below:

ZrL-Z ₂

(E) wherein L is as defined hereinbefore and Zi and Z ₂ are suitable leaving groups (such as halo (e.g. chloro or bromo)) to form a compound of formula II.

[0081] Step (i) of this process is defined hereinbefore.

[0082] in step (ii) of this process, the compound of formula i is suitably reacted with an organolithium compound (i.e. M is lithium). An example of a suitable organolithium compound is n-butyllithsum.

[0083] Suitably, in step (iii), and Z ₂ are the same and selected from chloro or bromo, especially bromo.

[0084] Any suitable solvent may be used for this process steps (ii) and (iii) of this process and a person skilled in the art will be able to select suitable reaction conditions.

[0085] Compounds in which L is -CH ₂ -CH ₂ - can also be formed by:

(i) reacting a compound of formula D1

D1

(wherein M is lithium, sodium, or potassium; and Ri and R ₂ are as defined hereinbefore) with BrCN in the presence of a suitable solvent to form a compound of formula E1 shown below

El

and

(ii) reacting a compound of formula E1 with C ₁₀ H ₈ . in the presence of a suitable solvent to form a compound of formula A

[0086] Compounds of formula D1 can be readiiy synthesized by techniques well known in the art.

[0087] Any suitable solvent may be used for step (i) of the above process. A particularly suitable solvent is diethyl ether.

[0088] Similarly, any suitable solvent may be used for step (ii) of the above process. A suitable solvent may be, for example, toluene, THF, D F etc.

[0089] For the avoidance of doubt, the C ₁₀ H ₈ . reagent used in step (si) of the above process is lithium, sodium or potassium naphthalenide. In an embodiment, C ₀ H ₈ .M is sodium naphthalenide.

[0090] The process steps (ii) and (iii) are defined further in the art. For example, reference can be made to WO201 1/051705 (see page 11 , line 22 to page 14, line 13 and the examples - page 17, line 1 1 to page 19, line 1 ), the entire contents of which are hereby incorporated by reference.

[0091] In addition, a process for the synthesis of a di-sodium ethylene-bis- hexamethyiindenyl ligand is described in J, Organomet. Chenri., 694, (2009), 1059-1068.

[0092] According to a fifth aspect of the present invention there is provided a process for forming a compound of formula Ml

(HI)

wherein Ri , F and L are as defined herein; X is zirconium, hafnium or titanium;

Y is selected from halo, hydride, a phosphonated or sulfonated anion, or a {1-6C)alkyl, (1 -6C)alkoxy, aryi or aryloxy group which is optionally substituted with halo, nitro, amino, phenyl, (1 -6C)alkoxy, or Si[(1-4C)aikyl] ₃ .

wherein the process comprises:

(i) forming a compound of formula II by the process defined above;

(ii) reacting the compound of formula II with a compound of the formula:

X(Y) ₂ (Z ₃ ) ₂

wherein X and Y are as defined above and Z ₃ is a suitable leaving group (e.g. chloro).

[0093] Step (i) of this process is defined above.

[0094] Step (ii) of this process typically involves forming a compound for formula lla:

wherein R-i , R _2l M and L are as defined above;

prior to the reaction with X(Y) ₂ (Z ₃ ) ₂ .

[0095] Suitable techniques for forming compounds of the formula lla are known in the art (see for example, WO201 1/051705). Suitably, the compound of formula lla is formed by reacting a compound of formula i! with a compound MQ as defined hereinbefore (e.g. n- butyilithium).

[0096] In step (ii) of this process, Y is a Hgand as defined herein and Z ₃ is suitably a haiide, such as bromo or chioro, especially chloro.

[0097] In an embodiment, Y and Z ₃ are the same and are suitably a haiide, such as bromo or chloro, especially chloro. Once the compound of formula III has been formed, the compound may be reacted to replace the Y groups with another Y group as defined herein other than halide.

[0098] Suitably, M is Li in step (ii) of the process defined above and the compound of formula lla is formed by reacting the compound of formula II with an organolithium compound of the formula MQ.

[0099] in an embodiment, the compound X{Y) ₂ (Z ₃ ) ₂ is provided as a solvate. In particular, the compound may be provided as X{Y)2( ₃ )2.THF _P! where p is an integer (e.g. 2).

[00100] Any suitable solvent may be used for step (ii) of the process defined above. A suitable solvent may be, for example, diethyl ether, toluene, THF, dichloromethane, chloroform, hexane DMF, benzene etc.

[00101] A person of skill in the art will be able to select suitable reaction conditions (e.g. temperature, pressures, reaction times, agitation etc.) for such a synthesis.

Applications

[00102] As previously indicated, the compounds of formula I are extremely important precursors for the formation of ligands of formula !l and metallocene catalysts of formula ill defined herein. The catalysts of formula III are particularly useful for the polymerisation of polyethylene.

[00103] As discussed hereinbefore, these catalyst compounds exhibit superior catalytic performance when compared with current metallocene compounds used in the polymerisation of a-olefins. In particular, when compared with current metallocene compounds used in the polymerisation of a-olefins, the compounds of the invention exhibit significantly increased catalytic activity. Moreover, polymers produced by a-olefin polymerization in the presence of compounds of the invention are typically of a higher molecular weight than polymers prepared using other catalysts, without an attendant increase in polydispersity. Such materials are highly valued by industry.

[00104] Thus, the present invention also provides a compound of formula II! when prepared by the processes defined herein.

EXAMPLE

[00105] An example of the invention will now be described by reference to the accompanying figures, in which:

Fig. 1 shows the ¹ H NMR spectra of hexamethylindanone (lnd ^# =0); Fig. 2 shows the molecular structure of hexamethylindanone (!nd -O);

Fig. 3 shows the ¹ H NMR spectra of hexamethyiindene (lnd H); and

Fig. 4 shows the molecular structure of hexamethyiindene, (ind H).

Example 1

General reaction scheme:

ind*=0 lnd ^# H

96% yield 98% yield

[00106] 41.8 g tiglic acid [trans-2-methylbutenoic acid] {417 mmol, 1 eq.) was dissolved in 1 L DCM. To this mixture, 52.9 g oxaly! chloride (417 mmoi, 1 eq.) was added which was washed in with a 100 mL portion of dichloromethane (DCM). Five drops of N,N- dimethylformamide was pipetted into the vigorously stirred solution causing a large amount of effervescence. The reaction was left stirring under nitrogen for 12 h before cooling to 8 °C, 61 .2 g aluminium trichloride (459 mmol, 1.1 eq.) was quickly added under a flow of N ₂ , causing a small temperature rise and the resulting DCM slurry to become light orange. 50 g 1 ,2,3,4-tetramethy!benzene (TMB) (372 mmol, 0.90 eq.) was mixed with 100 mL DCM and transferred to a pressure-equalising dropping-funne!. The TMB solution was added to the stirred reaction mixture in a fast-dropwise manner effecting a colour change through dark-orange to red. After stirring for a further four hours at room temperature, a solution of 500 mL cone. HCI and 500 g ice was made-up and was transferred to the reaction mixture to quench it, dropwise at first and then more quickly over 10 minutes. This caused the dark-red slurry to decolourise to a Sight pink solution. The stirring was stopped and the DCM layer was decanted before extracting the aqueous layer with 500 mL DCM twice more. The combined organic layer was washed with 500 mL deionised water, drying with magnesium sulfate, filtering and reducing in vacuo (40 °C, 550 mbar). The product was obtained as a light brown oil in 96 % yield (77.25 g, 357 mmol).

[00107] The proton NMR for the lnd ^# =0 is shown in Figure 1 and the molecular structure is shown in Figure 2.

[00108] 00 mL LiAIH ₄ (2.0 M in THF; 200 mmoi, 0,5 eq.) was combined with 100 mL dry, degassed THF and the mixture was cooled to 8 °C under N ₂ . 86.53 g lnd =0 (400 mmoi, 1 eq.) was dissolved in 150 mL dry, degassed THF and this was added to the stirred reaction mixture in a fast dropwise manner over the course of 10 minutes causing a small rise in temperature. The reaction was stirred for four hours before careful, portionwise quenching with 14.4 mL H ₂ 0 (800 mmol, 2 eq.) over approximately 30 minutes. 3 mL cone. H ₂ S0 ₄ (>95 %; 2 mol, 5 eq.) was added, slowly at first, causing the colour to change to a medium- dark grey over 30 minutes. The reaction was quenched with an additional 500 mL H ₂ 0 and extracted with DCM (3x 500 mL). The combined organic layer was washed with a further 500 mL H ₂ 0, dried over magnesium sulphate and reduced in vacuo (40 °C, 250 mbar), affording the product as a dark brown oil in 98 % yield (78.51 g, 392 mmol).

[00109] The proton NMR for the lnd H is shown in Figure 3 and the molecular structure is shown in Figure 4.

EXAMPLE 2

This synthesis is based on R, = CH ₃ and R ₂ = C ₂ H ₅

Synthesis of 3-ethyl-tigloyl chioride

(E)-2-methylpent-2-enoyl chloride

[00110] One equivalent of oxalyl chloride (26.45 g, 208 mmol) was added to a 2 L reaction vessel containing one equivalent of (E)-2-methylpent-2-enoic acid (23.85 g, 208 mmol) in DCM (500 mL) under a flow of N ₂ . While stirring, five drops of dry D F were pipetted Into the mixture creating effervescence. The reaction was left in a state a reflux for 2 hours. An aliquot was taken after 90 minutes showing that the reaction had gone to completion.

[00111] ¹ H NMR (CDC1 ₃ ): δ 1.08 (t, 3H, J = 7.6 Hz, e _b ), δ 1.88 (q, 3H, J = 1.0 Hz, Me _a ), δ 2.26 (quinq, 2H, J = 7.5, 0,9 Hz, CH ₂ ), δ 6.87 (tq, 1 H, J = 7.4 Hz, 1.3 Hz, vinylic-H)

[001 2] ¹³ C{ ¹ H} NMR (CDCI ₃ ): δ 12.57 (Me _b ), δ 13.23 (Me _a ), δ 22.93 (CH ₂ ), δ 154.23 (Vinylic-H) [00113] Synthesis of (lnd ^{3 Ethyi} )=0

3-ethyl-2,4,5,6,7-pentamethyl- 2,3-dihydro-1 H-inden-1 -one

[00114] The reactor was cooled to 8°C and allowed to equilibrate. 1 .1 equivalents of aluminium trichloride (30.6 g, 230 mmol) was added, under a flow of N ₂ , to the reactor. The mixture changed from a pale yellow to a deep orange almost instantly. 0.9 equivalents of tetramethylbenzene (25.0 g, 176 mmol) was diluted in 100 mL DCM and transferred to a pressure equalising funnel. This mixture was added to the reaction vessel dropwise over 15 minutes where a colour change from deep orange to blood red was observed. The solution was then left to stir for two hours, after which a solution of 00 mL cone. HC! and 100 g ice was made up and used to quench the reaction. The reaction mixture changed colour from blood red to a light orange solution during this workup. The product was extracted with DCM (3 x 100 mL) and the combined organic layer washed with deionised water (3 x 100 mL) before being dried using anhydrous MgS0 ₄ . This was filtered and the DCM solvent removed in vacuo to afford a beige solid in 100% yield (41 .8 g, 214 mmol).

[00115] ¹ H NMR (CDCl ₃ ): δ 0.56 (t, 3H, J = 7.5 Hz, Me _b ), δ 1 .28 (d, 3H, J = 7.2 Hz, Me,),

[00116] δ 1 .70 (m, 2H, CH ₂ ) δ 2.23 {s. 3H, Ar- e), δ 2.28 (s, 3H, Ar-Me), δ 2.28 (s, 3H. Ar-Me), δ 2.62 (s, 3H, Ar-Me), δ 2.74 (quin, 1 H. J = 7.3 Hz, CH), δ 2.74 (quin, 1 H, J = 7.3 Hz, CH), δ 3.45 (ddd, 1 H, J = 7.4, 6.1 , 3.6 Hz, CH)

[00117] MS (ESI): found 231 .17446; calculated 231 .17434.

Synthesis of (lnd ^{# 3 ethyl} )H

1-ethyl-2,4,5 _¾ 6J-pentamethyl-1 H-indene

[001 8] One equivalent of S-ethyW^^.ej-pentamethyl^.S-dihydro-I H-inden-l -one (22.4 g, 97 mmol) was added to 50 mL of dry, degassed THF in a schlenk tube. 0.5 equivalents of LiAIH ₄ (24.2 mL, 48 mmol) were added dropwise over 30 minutes and the resultant mixture left to stir for 2 hours under nitrogen. This caused the reaction mixture to turn light orange. The schlenk was cooled to 0°C and the reaction quenched by adding one equivalent of deionised water (1.74 mL, 97 mmol) dropwise. Upon addition of five equivalents of cone. H ₂ S0 ₄ (26.1 mL, 483 mmol) dropwise over 20 minutes the reaction mixture turned dark brown. The resultant solution was transferred to a 2 L reaction vessel and stirred for 30 minutes under a flow of N ₂ . The reaction was then quenched with 250 mL deionised water and extracted with DCM (3 x 500 mL). The combined organic layer was washed with deionised water (3 x 100 mL), dried over anhydrous MgS0 ₄ , filtered, and the solvent removed in vacuo to give a light brown solid (16.8g, 78 mmo!) in 80.6% yield.

[00119] ¹ H NMR (CDCI ₃ ): δ 0.46 (t, 3H, J = 7.4 Hz, Me _b ), δ 1 .97 (dqd, 1 H, J - 13.9, 7.4, 3.7 Hz, CH), δ 2.09 (d, 1 H, J = 0.8 Hz, Me _a ) 6 2.14 (m, 1 H, CH), δ 2.29 (s, 3H, Ar- e), δ 2.29 (s, 3H, Ar-Me), δ 2.36 (s, 3H, Ar-Me), δ 2.37 (s, 3H. Ar-Me), δ 3.36 (t, 1 H, J = 4.5 Hz, CH), 6 6.62 (quin, 1 H, J = 1 .5 Hz)

[00120] MS (ESi): found 215.17966; expected 215, 17943.

Synthesis of lnd ^# ' ^{3 ethyl} Li

1 -ethyl-2,4,5,6,7-pentamethyl

[00121] indenyllithium

[00122] One equivalent of 1-ethyl-2,4,5,6,7~pentamethy!-1 H-indene (16.8 g, 78 mmol) was dissolved in 50 mL DCM and transferred to a schlenk tube. The solvent was removed in vacuo before 100 mL pentane was added. 1 .1 equivalents of n-butyllithium (34.5 mL, 86 mmol) was added dropwise, at 0°C, to the dark brown mixture while stirring. The solution was allowed to warm up to room temperature and left stirring for 16 hours. The resulting yellow suspension was filtered on an air sensitive frit. The powder was washed with pentane (2 x 50 mL) and then dried under vacuum to form a white soiid in 52.4% yield (9.05 g, 41 mmol)

[00123] H NMR (C ₅ D ₅ N): δ 1.47 (t, 3H, J = 7.3 Hz, Me _b ), δ 2.45 (s, 3H, Ar-Me), δ 2.46 (s, 3H, Ar-Me), δ 2.65 (s, 3H, Ar-Me), 6 2.66 (s, 3H, Ar-Me), δ 2.89 (s, 3H, Me _a ), δ 3.31 (q. 2H, J = 7.3 Hz, CH ₂ ), δ 6.37 (s, 1 H, Ar-H)

[00124] ⁷ Li NMR {C ₅ D ₅ N): δ 1.06 (s) Synthesis of (lnd ^{* 3 et y,} ) ₂ ZrCI ₂

[00125] Two equivalents of l d ^,3"ethyl Li (3 g, 13.6 mmol) were added to one equivalent of ZrCI ₄ (1.59 g, 6.84 mmol) in a schienk tube inside a glovebox, and were stirred in 100 mL benzene under nitrogen for 16 hours at room temperature. The mixture was allowed to settie, and the mixture filtered. The solution was dried to afford an orange solid in 27.0% yield (1.09 g, 1.85 mmol). This solid comprised an equal mixture of both rac- and meso- isomeric forms which proved inseparable by fractional crystallisation from hexane, pentane, Et ₂ 0 and benzene. A further recrystallization from toluene yielded a light yellow precipitate of rac-(lnd ^{* ethy!} ) ₂ ZrCI ₂ which was isolated.

[001261 H NMR (C ₆ D ₆ ): δ 1.00 (t, 6H, J = 7.6 Hz, Me), δ 1.58 (s, 6H, Ar-Me), δ 2.09 (s, 6H, Ar-Me), δ 2.16 (s, 6H, Ar-Me), δ 2.38 (s, 6H, Ar-Me), δ 2.60 (s, 6H, Ar-Me), δ 2.81 (dq, 2H, J = 15.3, 7.7 Hz, CH ₂ ), δ 3.31 (dq, 2H, J = 15.1 , 7.5 Hz, CH ₂ ), δ 6.09 (s, 2H, Ar-H)

[00127] The features disclosed in the foregoing description, in the claims and the accompanying drawings may, both separately and in any combination, be material for realizing the invention in diverse forms thereof.