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THE PATENTS ACT 1970 [39 OF 1970]
&
THE PATENTS RULES, 2003

COMPLETE SPECIFICATION
[See Section 10; rule 13]
"A PROCESS FOR THE PREPARATION OF l,4-BIS(HYDROXYMETHYL) 2,3,5,6-TETRAFLUOROBENZENE"

SYNGENTA LIMITED, of Fernhurst, Haslemere, Surrey GU27 3JE, England

GRANTED
The following specification particularly describes the invention and the manner in which it is to be performed:
8-2-2006
8 FEB 2006

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The present invention relates to a process for the preparation of 1 4-Bis(Hydroxymethyl) 2,3,5,6-Tetrafluorobzene

The present invention relates to a process for making polyfluorinated benzyl alcohols which are useful in the synthesis of pyrethroid pesticides.
Esters of is-3-(baloalkenyl)-2,2-drmethylcyclopropanecarboxy c acid with 4-methyl-2,3 5,6-tetrafluoroberi2yl alcohol, in particular tefluthrin [2,3,5,6-tetrafluoro-4-methyIbenzyl cis-3-((Z)-2-chloro-3,33-triiluorpprop-l-enyl)-2,2-dimethylc3'clopropane carbbxylate] are important insecticidal and acaricidal products. It is thus desirable to have an industrially acceptable.and efficient process for making the necessary intermediates such as 4-metriyl-2,3,5,6-tetrafluoroben2yl alcohol.
Known processes for making of 4-methyl-2,3,5,6-tetrafluoroben2yl alcohol are described in DE3714602, GB2155464 and EP31199 but the processes involve reduction of the parent benzoic acids or acid halides using expensive reagents such, as borohydrides, or lithiation of tetrafluorobenzene at very low temperature followed by methylation. These methods are not suited to industrial application as they involve the use of expensive reagents or require specialised low temperature conditions.
The applicants have found that these disadvantages may be avoided by preparing 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol from 1,4-bis(hydroxymethyl)-2,3,5,6-tetrafluorobenzene and have devised a practical and efficient process for the manufacture of both compounds on an industrial scale starting from the readily available compound 2,3,5,6-' tetrachloroterephthalonitrile.
There is therefore provided a method for producing l,4-bis(hydroxymethyI)-2,3.,5,6-.
tetrafluorobenzene comprising:
a) fluorinating 2,3,5,6-tetrachloroterephthalonitrile to obtain 2,3,5,6-tetrafluoroterephthalonitrile;
b) hydrogenating 2,3,5,6-tetrafluoroterephthalonitrile to give l,4-bis(arninomethyl)-2,3,5,6-tetrafluorobenzene; and
c) converting l,4-bis(aminomethyI)-2,3,5,6 etrafluorobenzene to l,4-bis(hydroxymethyl)-2,3,5,6-tetrafluorobenzene.
The fluorination of step a) is suitably carried out vising fluoride exchange agents such as alkali metal fluorides, for.example potassium fluoride and optionally a phase transfer catalyst, for example tetramethyl ammonium chloride (TMAC). The reaction is suitably
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carried out in a solvent. Suitable solvents are dipolar aprotic solvents such as dimethylfomamide. The reaction is suitably performed at temperatures between 100-150°C, preferably at 130-150°C and preferably under anhydrous conditions.
The hydrogenation process of step b) may be carried out according to any of the procedures in described in EP99622. A particularly suitable method employs hydrogen and a metal catalyst such as palladium. The reaction may be carried out at from 0°C to about 60°C and from ambient pressure to lObar of over pressure. Suitable solvents for use in the reaction include alcohols, carboxylic acids, such as formic acid, acetic acid, or mixtures of either class with water. A preferred solvent for the hydrogenation reaction is acetic acid or aqueous acetic acid. The mol ratio of acetic acid is suitably 2-10:1 but is preferably 4-6:1
Step c) is preferably performed by diazotisation and in-situ hydrolytic decomposition of the diazonium salt. The diazotisation process is suitably performed using aqueous sodium nitrite and an acid at a temperature of 0-100°C , preferably 50-80°C. The concentration of the amine in the reaction (prior to nitrite addition) is suitably 5 - 30%, preferably 5-15%. The mol ratio of nitrite to l,4-bis(aminomethyl)-2,3,5,6-tetrafluoroberizeneis suitably 2-5:1 but 2:1 is preferred. After completion of step c), the product may contain some esters (e.g. acetate esters) of the desired benzyl alcohol product. The acetate ester structures are shown below.
OCOCH3

It has been found advantageous to render the reaction mass alkaline and then heat it to hydrolyse the esters to the desired diol compound. Once the esters have all been hydrolysed, the reaction mass is adjusted to between pH 7-10, preferably to between pH 9-10 prior to extraction of the product into a solvent for purification or for use in subsequent processes.
In a further aspect of the invention the l,4-bis(hydroxymethyl)-2,3,5,6-tetrafluorobenzene from step c) may be converted to 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol by
i) halogenation of l)4-bis(hydroxymethyl)-2,3,5,6-tetrafluorobenzene to give a 2,3,5,6-tetrafluoro-4-(haIomethyl)benzyl alcohol; and
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ii) hydrogenation of the 2,3,5)6-tetrafluoro-4-(halomethyl)benzyl alcohol to give 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol.
The halogenation of step i) where the halo group is for example chloro or bromo is suitably carried out using halogenating agents such as aqueous hydrochloric acid or hydrobromic acid. The reaction is suitably carried out in two phases in the presence of a solvent. Suitable solvents are inert and water immiscible solvents, such as aromatic . hydrocarbons, for example toluene. The reaction is performed at a temperature between 50-150°C, preferably at 75-100°C.
The hydrogenation reaction of step ii) may be performed under process conditions similar to those for outlined for step b) above but in the presence of a base to absorb the liberated hydrogen halide. Suitable bases are alkali or alkaline earth metal hydroxides or carbonates or alkaline earth metal oxides. Suitable solvents are alcohols, esters or aromatic hydrocarbons.
In yet a further aspect of the invention, the 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol is reacted with cis-Z 3-(2-choro-l,l,l-trifluoro-2-propenyl)-2,2-dimethylcyclopropane carbonyl chloride
to give tefluthrin.
Suitable conditions for performing the reaction are described for example in EP-A-31199.
In one preferred embodiment of the invention, the 2,3,5,6-tetrafluoroterephthalonitrile is hydrogenated in a carboxylic acid solvent, for example acetic acid, and the hydrogenation mass is passed straight into the diazotisation stage (step c)) after screening, and no further acid is then required.

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In another preferred embodiment l,4-bis(hydroxymethyl)-2,3,5,6-tetrailuorobenzene from step c) is extracted from the reaction mass in a solvent such as methyl isobutylketone (MiBK), the solvent removed under reduced pressure and a second solvent is added, the second solvent being suitable for the halogenation reaction of step i). A suitable second solvent is toluene.
In a further preferred embodiment, the l,4-bis(hydroxymethyl)-2,3,5,6-tetrafluorobenzene from step c) is extracted directly into a solvent that is also used in the halogenation reaction of step i). Suitable solvents are those that are stable to aqueous acid, such as aromatic hydrocarbons (for example toluene, xylene or a halobenzene) or halogenated hydrocarbons (for example ethylene dichloride or perchloroethylene).
The following Examples illustrate the processes and the compounds of this invention. 1H NMR was carried out on a Bruker AS 200 (200 MHz 1H) spectrometer, using TMS as reference standard. Gas chromatography analyses were obtained with a Hewlett Packard 5890 Series H. Hydrogenation reactions under pressure were carried out in a 1 litre stainless steel autoclave, fitted with a gas-inducing turbine agitator at 1000 rpm. Hydrogen feed was through a dip-pipe via a Buchi gas controller type 6002, heating and cooling was controlled by a Jelabo FP40 bath. Palladium on carbon type 58 catalyst was supplied by Johnson Matthey Ltd.
EXAMPLE 1 This Example describes the preparation of l,4-bis(hydroxymethyl)-2,3,5,6-tetrafluorobenzene
Step a. Preparation of 2, 3 5,,6-tetrafluoroterephthalonitrile
Potassium fluoride (117.7 g) and DMF (330 g) were charged to a 1 litre jacketed flask fitted with a condenser, nitrogen blanket and external heating cooling coil. The mixture was agitated under a nitrogen atmosphere for 5 minutes after which time a sample (5 ml) was taken and analysed for water content to ensure that the reaction mixture contained <0.2 wt% ivater. 2,3,5,6-Tetrachloroterephthalonitrile (120 g) and tetramethylammonium chloride (1.55 were then charged and the reaction mixture heated to 115°C under agitation. The reaction was maintained at 115°C under nitrogen for 6 hours after which time a sample was taken to Ietermine if completion of reaction had been achieved (i.e. monochloro impurity was < 2%). the reaction mixture was further heated at 115°C for 30 minutes if necessary. The reaction vas cooled to 70°C and dropped out of the reaction vessel via the bottom run off valve into a

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stirred 2 litre beaker containing water (670 g) at ambient temperature. The resulting slurry was filtered and the filter cake water washed (3 x 300 ml). The 2,3,5,6-tetrafluoroterephthalonitrile was partially dried on the filter and discharged into a suitable storage vessel. The reaction produced 97.8 g of water wet paste, GC analysis showed a strength of 78.6 % giving a yield of 85.2 %.
Step b. Preparation of l,4-bis(aminomethyl)-2, 3, 4 ,5,6-tetrafluorobenzene Water (258 g), acetic acid (179 g), 2,3,5,6-tetrafluoroterephthalonitrile paste (90.6 g 100% wt.), wetting agent (Nopco 8050) (0.15 g) and 5% palladium/carbon catalyst, (1.8 g 100% wt.) were charged to the autoclave. The lid was sealed and the autoclave was initially purged with nitrogen to remove residual oxygen and then pressurised to 5 bar g. with hydrogen after which the gas controller was zeroed. The agitator was started and the pressure maintained at 5 bar g. automatically by the Buchi controller. The temperature was monitored manually and the reaction exotherm controlled by manual intervention using the external heating / cooling bath. The reaction temperature was initially at 5°C rising to 30°C over the first 120 minutes of hydrogen ingress. The hydrogen consumption was totalled by the Buchi gas controller, rhe reaction was continued until the consumption of hydrogen ceased (typically 4 hrs.). The residual pressure was released and the autoclave purged with nitrogen. The contents of he autoclave were discharged by the autoclave's bottom run-off valve, followed by a small ;vater wash. The spent catalyst was removed by filtration. The filtrates and filter-cake water vashes were combined and analysed for product l,4-bis(aminomethyI)-2,3,5,6-etrafluorobenzene. The reaction produced 83.4 g of diamine, this equating to a reaction field of 88.6%.
5tep c. Preparation of l,4-bis(hydroxymethyI)-2,3,4,5,6-tetrafluorobenzene 4-Bis(armnomethyl)-2,3,5,6-tetrafluorobenzene (68.6 g), acetic acid (104 g), water (451 g) ind a silicone-based defoaming agent (0.2 g) were charged to a 1 litre split neck reaction lask, agitation was maintained throughout. The flask was held at 25 °C and aqueous sodium litrite solution (36%, 134.2 g) was added over 90 minutes. The reaction temperature was acreased to 70 °C over the course of the addition. The reaction was held at 70 °C for a ixrther 30 minutes following completion of the nitrite addition. The reaction mass was ampled and analysed for residual sodium nitrite using starch-iodide paper. Upon onfirmation that excess sodium nitrite had been charged (starch-iodide paper turns blue) the taction was cooled to 60 °C. The by-product acetate esters of the product were next

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hydrolysed by treatment with sodium hydroxide. Sufficient 47% aqueous sodium hydroxide solution was charged to raise the pH to >11.5. The temperature was then raised to 90 °C and held for 30 minutes after which time the pH was re-checked to ensure it was > 11.5. If pH was not >11.5, further sodium hydroxide solution was added and agitation maintained for a further 30 minutes.- Reaction temperature was lowered to 60 °C and the pH adjusted to 9 by addition of hydrochloric acid. This solution was then extracted with 4-methylpentan-2-one (MiBK, 2 x 250 ml), the organic extracts were combined and analysed to show a 90% yield of l,4-bis(hydimymemyl)2,3,5,6-tetrafluorobenzene by quantitative GLC analysis.
EXAMPLE 2 This Example describes the preparation of 4-methyl-2,3,5,6-tetrafluoro-benzyl alcohol
Step i. Preparation of 2,3,,5,6-tetrafluoro-4-(bromomethyl)benzyl alcohol A solution of 80gms l,4-bis(hydroxymethyl)-2,3,5,6-tetrafluorobenzene in MiBK produced as in Example 1 was charged to a 1 litre reaction flask fitted for distillation (both reflux return and total take-off). The solvent was removed by distillation and then steam distillation. Toluene (303g) was added and residual water removed by azeotropic distillation. The solution was agitated and heated to 60 °C for 30 minutes and Silcolapse (0.2 g) and 48% aqueous hydrobromic acid (109.3 g) were added to the reaction mixture and this was heated to 95°C. The distillation apparatus was set to reflux return for the initial 30 minutes of reaction at 95 °C. After this time, the toluene water azeotrope was collected in a separator with the toluene layer being recycled back to the reaction vessel. The reaction was heated for 5.5 hours at 95°C with toluene recycle. The mixture was cooled to 55°C with water (150 ml) and 48% aqueous hydrobromic acid (36.6 g) being added. This separation mixture was stirred at 55 °C for 15 minutes and then allowed to settle for 30 minutes prior to the aqueous phase being removed. The remaining toluene/product layer was further washed with a pre-prepared mixture of water (150 ml) and 40% aqueous sodium acetate solution (36 g) this was stirred and settled prior to the aqueous buffer layer being discharged. The toluene layer was analysed for 2,3,5,6-tetrafluoro-4-(bromomethyl)benzyl alcohol product and gave a yield of 96.2%.
Step ii. Preparation of 4-methyl-2,3,5,6-tetrafluoro-benzyl alcohol The following procedure used a reducer which was a 1 litre glass autoclave, working volume 350-500mls fitted with a gas dispersion agitator (lOOOrpm), gas feed through a dip-pipe via a

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Buchi gas controller type 6002, heating and cooling was controlled by a Jelabo FP40 bath. Methanol (362 g), water (6g), 2,3,5,6-tetrafluoro-4-(bromomethyl)benzyl alcohol (95.1 g 100% wt.), magnesium oxide (18.1 g) and 5% palladium/carbon catalyst, Johnson Matthey Type 58, (0.8 g 100% wt.) were charged to the autoclave. The lid was sealed and the autoclave was initially purged with nitrogen to remove residual oxygen and then pressurised to 2.5 bar g. with hydrogen after which the gas controller was zeroed. The agitator was started and the pressure maintained at 2.5 bar g. automatically by the Buchi controller. The reaction temperature was controlled at 50 °C throughout reaction by means of the external heating / cooling bath. The hydrogen consumption was totalled by the Buchi gas controller. The reaction was continued until the consumption of hydrogen ceased (typically 60 to 90 minutes). The residual pressure was released and the autoclave purged with nitrogen. The contents of the autoclave were discharged by the autoclave's bottom run-off valve, followed by a small methanol wash (30 g). The spent catalyst and inorganic salts was removed by filtration with the filter cake receiving methanol washes (2 x 30g). The filtrates and filter-;ake washes were combined. On analysis the reaction had produced 60.4 g of 2,3,5,6-tetrafluoro^4-methylbenzyl alcohol, equating to a reaction yield of 89.4 %.
EXAMPLE 3 This Example describes the preparation of 2,3,5,6-tetrafluoro-4-methylbenzyl cisJ-3-XZ)-2-choro-3,3,3-1iifluoroprop-l-enyl)-2,2-dimethylcyclopropanecarboxylate cis-Z 3-(2-choro-l,lJl-trifluoro-2-propenyl)-2,2-dimethylcyclopropane carbonyl chloride 257 g) was charged to a reactor fitted with an agitator, thermometer, sub-surface nitrogen nlet and jacketed dropping funnel. Nitrogen sparging was applied to the acid chloride and naintained throughout subsequent processing. Molten 4-methyl-2,3,5,6-tetrafluorobenzyl icohol (188.1 g) was charged to the dropping funnel. The temperature in the funnel was naintained at 80°C. The alcohol was charged to the acid chloride mixture over three hours. The maximum reaction temperature allowed during the addition was 45°C. On completion if the addition the temperature of the reaction mass was raised to 95°C and held for 2 hours. SC analysis was used to determine if full conversion of acid chloride had occurred and that o excess reactants were remaining. The mixture was cooled to 60°C and the molten taction mass discharged, weighed and analysed. The reaction yielded 423.3 g of molten ,3,5,64e1xailuorc4-memylbenzylds-3-((Z>2-cmoro-3,3,3-trifluoroprop-l-enyl)-2,2-

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dimethylcyclopropane carboxylate, analysis against a known standard showed this material t< be 92.5 wt% giving an overall reaction yield of 96.5%.

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We CLAIM:
1. A process for the preparation of l,4-bis(hydroxymethyl)-2,3,5,6-
tetrafluorobenzene comprising:
a] fluorinating 2,3,5,6-tetrachloroterephthalonitrile in the presence of a fluoride exchange agent in an aprotic solvent at 100-150°C to obtain 2,3,5,6-tetrafluoroterephthalonitrile;
b] hydrogenating 2,3,5,6-tetrafluoroterephthalonitrile to give 1, 4-bis(arninornethyl)- 2,3,5,6-tetrafluorobenzzene; and
c] converting 1, 4-bis(arninomethyl)-2,3,5,6-tetrafluorobenzene to l,4-bis(hydroxymethyl)-2,3,5,6-tetrafluorobenzene by diazotization using aqueous sodium nitrite and an acid at a temperature of 0-100°C followed by in¬still hydrolytic decomposition of the resulting diazonium salt.
2. A process as claimed in claim 1, wherein it optionally comprises the
additional steps of
i] halogenation of l,4-bis(hydroxymethyl)-2,3,5,6-tetrafluorobenzene
using halogenating agents in the presence of water immiscible solvents at 50-150°C, to give a 4-(halomethyl)-2,3,5,6-tetrafluoro-benzyl alcohol where halo is chloro or bromo and
ii] hydrogenation of the 4-(halomethyl)-2,3,5,6-tetrafluorobenzyl
alcohol in the presence of a base to give 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol.
3. A process as claimed in claim 2, wherein it optionally comprises the additional step of reacting 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol with cis-Z 3-(2-chloro-1,1, l-trifluoro-2-propenyl)-2>2-dimethylcyclopropane carbonyl chloride to form tefluthrin.
4. A process as claimed in any one of claims 1 to 3, wherein the step of converting l,4-bis(arninomethyl)-2,3,5,6-tetrafluorobenzene to 1,4-bis(hydroxymethyl)-2,3,5,6-tetrafluorobenzene is followed by a hydrolysis
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faction to convert ester by-products to the required l,4-bis(hydroxymethyl)-2,3,5,6-tetrafluorobenzene.
5. A process as claimed in any one of claims 1 to 4, wherein the 2,3,5,6-
tetrafluoroterephthalonitrile is hydrogenated in a carboxylic acid solvent and
the hydrogenation mass is passed straight into the diazotization stage (step c)
after screening, such that no further acid is required.
6. A process as claimed in any one of claims 1 to 5, wherein the reaction
mass containing the l,4-bis(hydroxymehtyl)-2,3,5,6-tetrafluorobenzene is
adjusted to pH 7-10 and the l,4-bis(hydroxymethyl)-2,3,5,6-tetxafluorobenzene
is extracted into a solvent.
7. A process as claimed in any one of claims 2 to 6, wherein 1,4-bis(hydroxymethyl)-2,3,56,-tetrafluorobenzene from step c) is extracted from the reaction mass in a solvent such as methyl isobutylketone (MiBK), the solvent removed under reduced pressure and a second solvent is added, the second solvent being suitable for the halogenation of l,4-bis(hydroxymethyl)-2,3,5,6-tetrafluorobenzene to a 4-(halomethyl)-2,3,5,6-tetrafluoro-benzyl alcohol.
8. A process as claimed in any one of claims 2 to 7, wherein the 1, 4-bis(hydroxymethyl)-2,3,5,6-tetrafluorobenzene from step c) is extracted directly into a solvent that is also used in the halogenation of l,4-bis(hydroxymethyl)-2,3,5,6-tetrafluorobenzene to a 4-(halomethyl)-2,3,5,6-tetrafluoro-benzyl alcohol.
Dated this 8th day of April, 2003.
Of REMFRY & SAGAR ATTORNEY FOR THE APPLICANTS

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