GB2157694A - Benzyl alcohol derivatives useful in the preparation of pesticidal esters - Google Patents

Abstract

New intermediates of formula <IMAGE> wherein X represents hydrogen, halogeno or an alkyl group and Z represents hydrogen, an alkyl group or a cyano or ethynyl group which are useful in the preparation of the corresponding pesticidal esters.

Description

SPECIFICATION Intermediates useful in the preparation of pesticidal esters This invention relates to pesticides and is particularly concerned with new intermediates for pesticidal compounds. The pesticidal compounds, their preparation, pesticidal compositions containing them and their pesticidal use are described and claimed in patent publication No.2,113 674, from which this application is divided.

Since the discovery in the 1940's of the structure of the naturally occurring pyrethnin insecticides, much research and development work has been directed to the production of synthetic analogues thereof. The naturally occurring insecticides are esters of certain cyclopropane carboxylic acids. Initially, investigations were directed to the production of new esters of the same cyclopropane-carboxylic acids from which the naturally occurring products are derived, but subsequently, investigations have been directed to esters in which the cyclopropane-carboxylic acid part of the molecule was modified and, more recently, it has been found that valuable insecticidal compounds can be prepared which are esters not of cyclopropane- carboxylic acids but which are esters of a-substituted phenyl acetic acids.

In developing new analogues of the naturally occurring insecticides, attention has been directed to the production of compounds having improved pesticidal properties while, at the same time, having an acceptably low level of toxicity to mammals, fish etc., and a sufficient level of physical stability so that the compounds can be used agriculturally, as well as for domestic and horticultural uses, without the need for repeated applications of the compound during a growing season.

We have now found that compounds of a new structural type have a particularly valuable combination of biological and physical properties rendering them useful as pesticidal compounds.

Accordingly, the present invention provides a compound of the general formula:

wherein X represents hydrogen, halogeno or an alkyl group, Z represents hydrogen, an alkyl group or a cyano or ethynyl group and R represents the residue of a carboxylic acid RCOOH which is an acid forming a pesticidal compound when esterified with a-cyano- 3-phenoxybenzyl alcohol.

The compounds of the present invention may be regarded, structurally, as esters of the new alcohol of formula V

where X and Z are as defined above and alcohols of formula V, together with their ester-forming derivatives, form a further aspect of this invention.

In the compounds of formula I and V, it is preferred that X is hydrogen. When X is alkyl, it is preferred that this is an alkyl group containing 1 to 4 carbon atoms and is particularly a methyl group. When X is halogen, it is preferably chlorine but may also be bromine or fluorine.

In the compounds of formula I and V it is preferred that Z is H or CN.

It is also preferred that, in the compounds of formula I and V, that the 1-phenylvinyl or 1-phenyl-alkenyl or 1-phenylhalovinyl group be substituted at the 3- position on the benzyl ring.

In the compounds of formula I, R represents the residue of a carboxylic acid RCOOH which is an acid known to be capable of forming pesticidal compounds when esterified with o-cyano-3-phenoxybenzyl alcohol. There are a large number of carboxylic acids that are known to form pesticidal compounds of this type and these carboxylic acids fall, for the most part, into two clearly defined groups. The first group are the cyclopropane carboxylic acids which are the compounds where R is a group of the formula:

In formula II, R3 and R4 will normally be an alkyl group, usually the same alkyl group containing 1 to 4 carbon atoms and, as is well-known in the art, dimethyl substitution normally gives high activity.

R2 in formula II will normally be hydrogen or an alkyl group containing 1 to 4 carbon atoms and here, the experience of the art indicates that R2 will usually be hydrogen for maximum activity except in those compounds where R is also an alkyl group in which R2 preferably is an alkyl group, R1, R2, R3 and R4 all conveniently being the same alkyl group, e.g. methyl.

In formula II, Ri can be hydrogen or a substituted or unsubstituted acyclic or carbocyclic group. When Ri is an unsubstituted hydrocarbyl group, it can be a straight chain or branched saturated or unsaturated acyclic or carbocyclic group such as an alkyl group, an alkenyl or alkadienyl group or a cycloalkyl, cycloalkylalkyl or cycloalkylalkenyl group. These hydrocarbyl groups preferably contain up to 10, particularly up to 6 carbon carbon atoms.

When group R is substituted, it is preferably one of the hydrocarbyl groups mentioned above which is substituted by one or more halogeno groups which may be fluorine, chlorine or bromine or by an alkoxy or oximino group. When the substituents are two or more halogeno substituents, the halogeno substituents need not necessarily be the same halogen while when alkoxy groups are present, these preferably contain up to 4 carbon atoms and will normally be methoxy groups.

One particularly valuable structure for the group.R1 is of-formula IV

where R7 and Ra, which may be the same or different, are each alkyl group containing 1 to 4 carbon atoms, a trifluoromethyl group or a halogeno group, which may be the same or different and are preferably fluorine, chlorine or bromine. One of R7 and Ra may also represent hydrogen or a phenyl or substituted phenyl group. Alternatively, R7 and Ra may together form a straight or branched substituted or unsubstituted saturated or unsaturated divalent hydrocarbon chain which may be substituted by one or more hetero atoms e.g.O, N or S, so that R7 and Ra together with the carbon atoms to which they are attached forms a carbocyclic or heterocyclic or heterocyclic ring which will preferably contain 5 to 7 ring atoms, optionally 1 or 2 carbon-to-carbon double bonds and optionally one or more alkyl (C,-C4) or halogeno substituents on the cycloaliphatic ring. Other compounds of interest are those in which R is a group of the structure

where the dotted line represents an optional double bond and X represents H or halogen such as chlorine.

Specific cyclopropane carboxylic acids from which the compounds I of the present invention may be structurally derived include the following: Chrysanthemic acid including particularly (1 R)-trans chrysanthemic acid; Pyrethric acid; Dimethylcyclopropane carboxylic acid; Trimethylcyclopropane carboxylic acid; Tetramethylcyclopropane carboxylic acid; 2,2-Dimethyl-3-(cyclopentylidenemethyl)cyclopropane carboxylic acid; 2,2-Dimethyl-3-(dibromovinyl)cyclopropane carboxylic acid; particularly the (IR)-cis isomer thereof; 2,2-Dimethyl-3-(dicnlorovinyl)cyclopropane carboxylic acid; particularly the (1 R)-cis isomer thereof; 2,2-Dimethyl-3-(1 ,2,2,2-tetrabromoethyl)cyclopropane carboxylic acid; 2,2-Dimethyl-3-(1 ,2-dibromo-2,2-dichloroethyl)cyclopropane carboxylic acid; ; 2,2-Dimethyl-3-(2-chloro-3,3,3-trifluoropropenyl)- cyclopropane carboxylic acid; 2,2-Dimethyl-3-(tetrahydro-2-oxo-thien-3-ylidenemethyl)- cyclopropane carboxylic acid.

the second major class of carboxylic acids from which the esters of formula I may be structurally derived are the a-substituted aryl acetic acid esters. In these compounds R in formula I will normally be of the structure Ill

wherein Ar represents an aryl residue, R5 represents a saturated or unsaturated straight chain or branched acyclic or cyclic hydrocarbon residue and Re represents hydrogen or one or more alkyl, alkoxy (including substituted alkoxy such as OCF3 and OCHF2) or halogeno substituents.

Ar will normally be an aryl residue based on a benzene ring although other aryl residues, e.g. polynuclear residues are also of interest. R5 will normally be a saturated straight or branched chain hydrocarbon group, particularly an alkyl group containing up to 8 carbon atoms and it is often desirable that this alkyl group should contain at least one secondary carbon atom particularly when that secondary carbon atom is directly bonded to the carbon atom directly bonded to the Re substituted aryl group. Thus R5 is preferably an isopropyl group or a secondary butyl group. R5 can also be a cycloaliphatic residue, again preferably containing a secondary carbon atom located immediately adjacent to the carbon atom carrying the R6 substituted phenyl group, e.g.Rs may be a cyclopropyl group or an alkyl substituted cyclopropyl group.

Rs can also be a cycloalkylalkyl group.

R6 is preferably one or more halogeno or halogen- containing substitutents, e.g. F, Cl, Br or OCHF2 or OCF5 and, when more than one halogeno or halogen- containing substituent is present, they will normally be but are not necessarily the same halogen. When R6 is an alkyl or alkoxy group, these preferably contain up to 4 carbon atoms and again, when more than one such group is present, they need not necessarily be the same groups. When only one substituent R6 is present, it is preferably present in the para-position. When more that one Re substituent is present, the para-position is preferably substituted together with one or more of the ortho and meta positions.

Another class of carboxylic acids from which the esters of the present invention may be structurally derived are a-substituted arylamino acetic acids of the type

where R5, Re and aryl are as defined above.

Specific a-substituted penyl acetic acids from which esters of the formula I may be structurally derived include: a-lsopropyl-p-chlorophenyl acetic acid; a-Cycloprnpyl-p-chlornphenyl acetic acid; a-Cyclopropyl-p-methylpehnyl acetic acid; a-lsopropyl-p-(difluoromethoxy)-phenyl acetic acid; a-lsopropyl-(2-chloro-4-trifluoromethyl anilino) acetic acid.

The compounds of the invention may exhibit geometrical and/or optical isomerism. Compounds of the invention in which X represents alkyl or halogen can exist in the form of E or Z isomers in view of the asymmetric substitution on the carbon atoms linked by the olefinic bond and the present invention includes both the substantially pure Z isomers as well as mixtures thereof.

Compounds of the invention in which Z represents CH3, CN or ethynyl exhibit optical isomerism in that the carbon atom bearing the substituent Z can exist in the R orS configuration and the present invention includes compounds in which the configuration is substantially completely R or in which the configuration is substantially completely S or mixtures thereof.

Compounds of the invention in which R represents a substituted cyclopropane residue of formula II can exist in the form of both geometrical and optical isomers. This is because of the unsymmetrical substitution at C1 and Cs of the cyclopropane ring. Compounds of the present invention include those isomers in which the hydrogen atoms at C1 and C3 of the cylcopropane ring are substantially completely in the cis configuration or substantially completely in the trans configuration or mixtures thereof. The present invention also includes compounds in which the configuration at C1 is substantially completely S and mixtures thereof.In the compounds of the invention in which R represents a group of formula 11, the optical configuration at C1 and Cs cannot vary independently of the geometrical configuration of the hydrogen atoms at C1 and C3 of the cyclopropane ring. The effect of this is that the configuration of the cyclopropane ring can be defined uniquely by specifying the optical configuration at C1 and the geometrical configuration of the hydrogen atoms at C1 and Q and, for definition purposes, we have adopted nomenclature of the form (1R)-cis, (1 R)-trans etc. it being unnecessary to specify the optical configuration of C3 which is fixed once the other two variables are defined.Adopting this nomenclature avoids the confusion which can arise by having to designate either R or S to the same optical configuration at C3 depending upon the nature of the substituents on the cyclopropane ring and even those on the side chain.

When R is a group of formula II in which R1 is a group of formula IV in which the substitution about the ethylenic bond is asymmetrical, that is to say R7 + Re then the configuration of this part of the molecule can be substantially completely in the E form or substantially completely in the Z form or a mixture thereof.

When R is a group of formula lil, the carbon atom to which R5 is bonded can exist substantially completely in the S configuration or substantially completely in the R configuration or can be a mixture of the two forms.

The compounds of the present invention can be in the form of single isomers but, having regard to the fact that the compounds have at least one and frequently more than one centre of assymetry, the compounds of the invention will normally be in the form of isomer mixtures although these isomer mixtures can be optically active and/or substantially completely in one geometric form.

The compounds of the present invention can be prepared by an esterification involving the reaction of an alcohol or formula IV or an esterifiable derivative thereof with a carboxylic acid of formula RCOOH or an esterifiable derivative thereof. It is usually convenient in practice either to react a salt of the caroxylic acid, e.g. a silver or triethylammonium salt with a benzylhalide derivative, that is to say a 1-phenylvinylbenzyl halide.

Alternatively, the esters of the invention can be prepared by transesterification by reacting a C1-C6 alkyl ester of the carboxylic acid with the benzyl alcohol of formula V in the presence of a basic transesterification catalyst. This method is not usually satisfactory where the molecule contains another base- sensitive residue, e.g. where the carboxylic acid is pyrethric acid.

The esters of the present invention may also be prepared by converting the carbonyl group in the corresponding benzoylbenzyl carboxylate of the formula

into a vinyl group either by a Wittig reaction or by the Grignard synthesis described below followed by dehydration. The key intermediate to the synethesis of the pesticidal esters of the present invention are the new alcohols of formula V

The synthesis of the new alcohols can be achieved either by a Wittig reaction or by a Grignard reaction followed by dehydration to convert the carbonyl group into a benzoylbenzyl alcohol (possibly having a protected alcohol group) to form a 1-phenylvinyl benzyl alcohol having a protected alcohol group and then removing the protected alcohol group.

The synthesis produces alcdhols of formula V in which Z = H.

Alcohols of the invention of formula V in which Z represents methyl, cyano or ethynyl are conveniently prepared via the corresponding benzaldehyde of formula VII

by reacting the aldehyde group with either methyl magnesium iodide or hydrogen cyanide or ethynyl magnesium bromide to give the methyl, cyano or ethynyl substituted benzyl alcohol.

The benzaldehyde of formula VII may be prepared from the corresponding methyl-substituted benzophenone. The methyl substituent is first subjected to side-chain bromination, e.g. by treatment with bromine and the resulting dibromomethyl benzophenone hydrolysed with stronger mineral acid, e.g.

sulphuric acid to give the corresponding benzoyl-benzaldehyde. The aldehyde group can then be protected, e.g. as an acetal or ketal and the unprotected carbonyl group linking the two aromatic rings then reacted with methyl magnesium idoide under the conditions of the Grignard synthesis followed by dehydration or reacted with a Wittig regaent to convert that carbonyl group into a corresponding 1- phenylvinyl benzaldehyde in which the aldehyde group is protected. The protecting group can then be removed to give the 1-phenylvinyl benzaldehyde which can then be reacted with methyl magnesium iodide, hydrogen cyanide or ethynyl magnesium bromide to give the correspondingly a-substituted 1-phenylvinyl benzyl alcohol. Protection of the aldehyde group is not necessary when, for example, an a-methyl-benzyl alcohol product is required. In such a case, a benzoyl-benzaldehyde can be reacted with 2 equivalents of, for example, methyl magnesium idoide in accordance with the reaction:

The Grignard technique can also be used directly on (x-substituted benzoyl-benzoyl alcohols, e.g. in accordance with the reaction:

Any desired substitution on the 2-carbon atom of the vinyl group can be carried out by the procedures described above.

One or more of the pesticidal esters of formula I can be formulated with an inert carrier or diluent to give pesticidal compositions and such compositions form a further aspect of the present invention. These compositions can be in the form of dusts and granual solids, wettable powders mosquito coils and other solid preparations, or as emulsions, emulsifiable concentrates, sprays and aerosols and other liquid preparations after the addition of the appropriate solvents, diluents and surface-active agents.

The pesticidal compositions of the invention will normally contain from 0.001 to 25% by weight of the compound of formula I but the compositions can contain higher concentrations of active ingredient of formula I e.g. up to 95% for compositions to be sold as concentrates for dilution before use by the ultimate user.

The compositions of the invention can include diluents such as hydrocarbon oils, e.g. xylene or other petroleum fractions, water, anionic, cationic or non-ionic surface- active agents, anti-oxidants and other stabilisers as well as perfumes and colouring matters. These inert ingredients may be of the type and in proportions such as are conventionally used in pesticidal compositions containing pyrethroid-like compounds.

In addition to these inactive ingredients, the compositions of the present invention may contain one or more further active ingredients which may be other pesticidal compounds of the pyrethroid type or of other types and the composition may also include synergists of the type known to be capable of synergising the activity of natural pyrethrin and pyrethroid-like insecticides. Synergists of this type include piperonyl butoxide, tropital and sesamex.

The compounds of formula I can be used to control pest infestation in the domestic, horticultural or agricultural or medical including veterinary areas. The compounds or compositions of the invention can be used to combat pest infestation by treating pests or surfaces or environments susceptible to pest infestation with effective amounts of the active compounds of formula I or of compositions containing them. For example, they may be used in a domestic environment for spraying rooms to combat infestation with houseflies or other insects, they can be used for treatment of stored dry crops or cereals to combat infestation by insects or other pests, they can be used to spray growing crops, e.g. cotton or rise to combat infestation by common pests and finally, they can be used in a medical or veterinary field, e.g.

as a cattle spray to prevent or treat infestation by insects or other pests.

The following Examples are given to illustrate the invention. Temperatures are in "C.

Example 1 3-(1-phenylvinyl}-benzyl (/I?,tra ns)-chrysanthemate (a) A mixture of 3-benzoylbenzyl alcohol (a.82 g, 5.0 mmol), dihydropyran (0.84 g, 10 mmol) and 'Amberlyst' 15 (0.4 g, 1.34 meq) in dry diethyl ether (60 cma) was stirred at room temperature for 1 hour. The resin was filtered off and the solvent and excess dihydropyran removed in vacuo. The residue (1.68 g (100%) was 2-(3-benzoylbenzyl)-tetrahydropyran, n020 1.5672.

(b) To a stirred suspension of methyltriphenyl-phosphoniuum iodide (5g, 12.4 mmol) in dry ether (150 cm3) under nitrogen at room temperature was added n-butyllithium in hexane (1.6M, 7.5 cma, 12 mmol) over 10 minutes. After 30 minutes the mixture was cooled in an ice bath and the product from (a) above (1.89, 6.1 mmol) in dry ET2O (20 cm3) was added dropwise and the mixture allowed to warm up to 20"C over 3 hours. Water (200 cm3) was added and the reaction mixture filtered after stirring for 10minutes.

The ethereal layer was separated off and the aqueous layer extracted twice with diethyl ether. The combined extracts were dried over an hydros Na2SO4 and the solvent removed in vacuo. The residue was purified by HPLC on silica gel (Merck Lichroprep Si60, 15-25m, 100g) eluted with 10% ether/petrol (60 80 ) to give 2-(3-(1-phenylvinyl)- benzyl)tetrahydropyran. Yield 0.8 g (44.4%) nD 1.5712.

(c) The product from (b) above (0.6 g, 2 mmol), 'Amberlyst' 15 (0.4 g, 1.34 meq) and methanol (20 cm3) were stirred at 50 for 1 hour. After cooling to room temperature, the resin was filtered off and the solvent evaporated off in vacuo to give 3-(1-phenylvinyl)benzyl alcohol. Yield 0.42 g (97.7%) n020 1.5915.

(d) (1 R,cis)-3-(2,2-dibromovinyl)-2,2-dimethyl- cyclopropanexarboxylic acid chloride (0.2 g, 0.63 mmol) was added to a stirred solution of the 3-(1-phenylvinyl)- benzyl alcohol (0.15 g, 0.7 mmol) and pyridine (0.06 g, 0.7 mmol) at 200C. After 4 hours, the mixture was passed through a column of alumina (10 g) and eluted with benzene (25 cm 3). The eluate was evaporated to dryness, finally at high vacuum and purified by tic on silica to give 3-(1-phenylvinyl)benzyl(1R,trans) chrysanthemate (Compound 1)(0.2 g 67%) n020 1.5604.

Example 2 The procedure described in Example 1(d) was repeated but replacing the chrysanthemic acid chloride by (1 R,cis)-2,2-dimethyl-3-(dibromovinyl)cyclopropane carboxylic acid chloride (dibromosanthemac acid) to give 3-(1-phenylvinyl) benzyl (1R,cis)-dibromosanthemate (Compound 2) n020 1.5986.

Example 3 3-{1-phenylvinyl)benzaldehyde (a) A solution of 3-methylbenzophenone (10 g, 51 mmol) in CC14 (40 cm3) was refluxed with stirring and illuminated with an infra-red heat lamp (275 w) while bromine (16.3 g, 102 mmol) in CC14 (50 cm3) was added dropwise. After 16 hours the clear solution was washed successively with water, saturated sodium bicarbonate, water and saturated sodium chloride. After drying the solution, the solvent was removed under vacuo to give 3-dibromomethylbenzophenone. Yield 17.3 g (96%), 98% purity.

(b) Concentrated sulphuric acid (14.5 cm3) was added to a stirred mixture of the dibromide obtained in (a) above (9.65 g, 27.3 mmol) in water (0.7 cm3) and heated initially to 70"C and then to 110 C whilst under reduced pressure (20 mmHg) with an air bleed. After 90 minutes, the mixture was cooled, poured onto ice and after warming to 20 C, extracted with diethyl ether (200 cm3 x 3). The combined extracts were washed with saturated sodium bicarbonate, water and saturated sodium chloride. After during with anhydrous Na2SO4, the solvent was evaporated off and the residue distilled to give 3-benzoylbenzaldehyde. Yield 4.8 g (84%) b. pt. 140-150 /0.04 mmHg.

(c) To a stirred solution of benzoylbenzaldehyde (2 g, 10 mmol) and 1,2-bis-(trimethoxysiloxy) ethane (2.3 g, 11 mmol) in dry dichloromethane (30 cm3) under N2 at room temperature was added trimethylsilylmethyl trifluoromethanesulphonate (5 drops). After stirring at 20"C for 48 hours, pyridine (3 drops) was added followed by saturated NaHCO3 (20 cm3) and diethyl ether (20 cm3). The resulting mixture was stirred for 30 minutes. The ethereal layer was separated off and the aqueous layer extracted twice more with diethyl ether. The combined extracts were washed with water, dried over a mixture of anhydrous Na2CO3 and anhydrous NazSO4 (1:1) and the solvent removed in vacuo to give 2-(3-benzoylphenyl)-1,3dioxolane, n3 1.5890.Yield 2.2 g (91.7%).

(d) To a stirred suspension of methyltriphenyl-phosphonium iodide (5 g, 12.4 mmol) in dry ether (150cm3) under nitrogen at room temperature was added n-butyllithium in hexane (15% w/w, 5g) over 15 minutes. After 30 minutes, the mixture was cooled in an ice bath and the dioxolane from (c) above (1.8 g, 7.1 mmol) dissolved in dry diethyl ether (10 cm3) was added dropwise. The cooling bath was removed and the mixture allowed to warm up to 20 C over 3 hours. Water (200 cm3) was added to the reaction mixture and filtered after stirring for 10 minutes. The ethereal layer was separated and the aqueous layer extracted twice with ether. The combined extracts were dried over an hydros Na2SO4 and the solvent removed in vacuo to give 2-(3-(1- phenylvinyl)phenyl)-1,3-dioxolane. Yield 1.54 g.

(e) The crude product from (d) above (1.54 g) was added to 10% H > SO4 (15 cm3l in tetrahydrofuran (15 cm3) and refluxed for 1 hour, cooled and poured onto water (200 cm3), then extracted with dichloromethane (x3). The combined extracts were dried and evaporated in vacuo. The product was purified by passing through a short column of silica gel eluting with ether to give 3-(phenylvinyl)-benzaldehyde.

Yield 0.77 g (60%). n030 1.6148.

(f) A mixture of the aldehyde from (e) above (0.77 g, 21 mmol), THF (10 cm3) sodium cyanide (0.6 g) and water (3 cm3) was stirred in an ice-bath and 40% sulphuric acid (1.8 cm3) added dropwise whilst maintaining the temperature below 5"C. After 1 hour, the cooling bath was removed and the mixture allowed to warm up to 20 over 1 hour. The mixture was poured onto water (200 cm3) and extracted with carbon tetrachloride (50 cm3 x 3). The combined extracts were washed with water, dried and the solvent evaporated off to give o-cyano-3-(1-phenyl-vinyl)benzyl alcohol. Yield 0.8 g (87%) nD 1.5935.

(g) The esterification procedure described in Example 1 (d) and 2 was repeated using the alochol obtained in paragraph (f) above to give o-cyano-3-(1-phenylvinyl)- benzyl (1R,trans) chrysanthemate (Compound 7) n030 1.5628 and or-cyano-3-(l-phenylvinyl)benzyl (1R-cis) dibromo-santhemate (Compound 8) n020 1.5872.

Example 4 a) a-Eth yn yl-3-b enzoylb enzyl alcohol Ethynylmagnesium bromide (11.2 mmol) in tetrahydrofuran (20 cm3) was added dropwise to a stirred solution of 3-benzoylbenzaldehyde (2 g, 9.5 mmol, prepared as in Example 3(b) in tetrahydrofuran (30 cm3) through which purified acetylene was being passed. After 2 hours, saturated ammonium chloride solution (200 cm3) was added, and the mixture extracted with ether (3 x cm3). The combined extracts were washed with saturated sodium chloride, dried over andyrous sodium sulphate, and the solvent removed in vacuo. The product was purified by thin layer chromatography on silica to give the titel alcohol, yield 1.1 g (49%) nD 1.6075.

b) c -Ethynyl-3-61-phenylvinyl)benzyl alochol To methyl magnesium iodide (1.4 g) in ether (25 cm3) was added a solution of o-ethynyl-3-benzoylben- zyl alcohol (0.5 g) in ehter (10 cm3) with stirring during 10 minutes at 20"C, then the mixture refluxed for 5 minutes and poured onto a mixture of 40% sulphuric acid (40 cm3), sodium thiosulphate (3 g) and tetrahydrofuran (20 cm3). After 16 hours at 20"C, this mixture was extracted with ether (3 x 150 cma), washed with sodium thiosulphate solution (2M), saturated sodium chloride, dried and finally evaporated to give the title product, yield 0.48 g (96%) n3 1.5942.

c) The procedure described in Example 1(d) and 2 was repeated using a-ethynyl-3-)1-phenylvi- nyl)benzyl alcohol in place of 3-(1-phenylvinyl)benzyl alcohol to give the a-ethynyl-3-(1-phenylvinyl)benzyl ester of (1R,trans) chrysanthemic acid, (Compound 5 n020 1.5568 and (1R,cis) dibromosanthemac acid (Compound 6) n3 1.5965.

Example 5 a) 3-( l-Phenyl-2-chloro vinyl)benzyl alcohol.

To a stirred suspension of (chloromethyl) triphenyl phosphonium chloride (2 g, 5.8 mmol) in ether (25 cm3) containing piperidine (0.51 g, 6 mmol) at 20"C was added butyl lithium (15%, 2.4 g, 5.6 mmol) in hexane over 15 minutes and then kept for 2 hours to generate the chloromethylene phosphorane. The mixture was cooled to -78 C, and 3-benzoylbenzyl acetate (1 g, 3.9 mmol, prepared from the alcohol and acetyl chloride by the esterification procedure of Example 1d) in ether (10 cm3) was added dropwise.

After 1 hour at -78C and 24 hours at 20"C, water (100 cm3) was added with stirring, and the mixture filtered. The ether layer, and extracts of the aqueous layer were combined, dried over anhydrous Na2SO4 and evaporated to dryness. After purification by t.l.c. on silica, the 3-(1-phenyl- 2-chlorovinyl)benzyl acetate, yield 0.26 g (23%) had n3 1.5912.

The above acetate (0.25 g, 0.9 mmol) in ether (20 cm3) was reduced by adding lithium aluminium hydride (0.05 g, 1.4 mmol) and stirring at 20"C for 1 hour. Water (0.05 cm3) was added, followed by 15% aqueous sodium hydroxide (0.05 cm3) and water (0.15 cm3). After stirring a further 10 minutes, the solution was filtered, and the filtrate evaporated in vacuo to give 3-(1-phenyl-2-chlorovinyl)benzyl alcohol, yield 0.21 g (98%) n020 1.6200.

b) The procedure described in Example 1(d) and 2 was repeated using 3-(1-phenyl-2-chlorovinyl)benzyl alcohol in place of 3-(1-phenylvinyl)benzyl alcohol to give the 3-(1-phenyl-2-chlorovinyl)benzyl ester of (1r,trans) chrysanthemic acid (Compound 11) n)' 1.5706 and (1R,cis) dibromosanthemic acid (Compound 12) nD 1.5962.

Example 6 3-(l-Phenylprnp- l-eny/)benzyl alcohol This alcohol n3 1.5725 was prepared by the procedure of Example 5(a) using the phosphorane generated from ethyltriphenylphosphonium iodide with butyliithium. The alcohol was then esterified with (1R,trans) chrysanthemic acid and (1R,cis)-dibromosanthemic acid by the procedure described in Examples 1(d) and 2 to give 3-(1-phenylprop-1-enyl)benzyl (1R,trans) chrysanthemate, (Compound 9) n3 1.5618 and (1R,cis) dibromosanthemate, (Compound 10) n1.5978.

Example 7 a) -Meth yl-3-( l-pheny/viny/)benzyl alcohol To methyl magnesium iodide (from magnesium and methyl iodide (2.9 g) in ether (10 cm3)), was added 3- benzoylbenzaldehyde (1 g, 4.8 mmol, prepared as in Example 3(b)). After refluxing for 10 minutes, the mixture was cooled, poured onto dilute sulphuric acid and extracted with ether (3 x 200 cma). The extract was washed with solutions of sodium thiosulphate and sodium chloride, then dried (anhydrous Na2SO4) and evaporated to a residue which was dissovled in a mixture of tetrahydrofuran (10 cma) and 40% sulphuric acid (10 cm3) for 10 hours. The mixture was poured onto water, and extracted with dichloromethane (3 x 50 cm3). The extract was dried and evaporated to give the title alcohol.Yield 1.05 g (98%) n 1.5978.

b) The procedure described in Example 1(d) and 2 was repeated using a-methyl-3-(1-phenylvinyl)benzyl alcohol in place of 3-(1-phenylvinyl)benzyl alochol to give the or-methyl3-(l -phenylvinyl)benzyl ester of (1R,trans) chrysanthemic acid (Compound 3) n3" 1.5588 and of (1R,cis)- dibromosanthemic acid (Compound 4) n020 1.5912.

The pesticidal activity of esters of formula I of the invention was assessed against houseflies and mustard beetles using the following techniques: Houseflies (Musca domestic Female flies were treated on the thorax with a one microlitre drop of insecticide dissolved in acetone.

Two replicates of 15 flies were used at each dose rate and 6 dose rates were used per compound under test. After treatment, the flies were maintained ata temperature of 20"C. + 1" and kill was assessed 24 to 48 hours after treatment. LD50 values were calculated in micrograms of insecticide per fly and relative toxicities were calculated from the inverse ratios of the LDso values (see Sawicki et al, Bulletin of the World Health Organisation, 35, 893, (1966) and Sawicki et e/, Entomologia and Exp. Appl. 10, 253, (1967)).

Mustard Beetles (Phaedon cochleariae Fab) Acetone solutions of the test compound were applied ventrally to adult mustard beetles using a micro drop applicator. The treated insects were maintained for 48 hours after which time kill is assessed. Two replicates of 40 to 50 mustard beetles were used at each dose level and 5 dose levels were used for each compound.

Again, LDso values were calculated and relative toxicities were calculated for the inverse ratios of LD50 (see Elliott et al, J. Sci. Food Agric. 20, 561, (1969)).

Relative toxicities were calculated by comparison with 5-benzyl-3-fu rylmethyl (1 R)-trans-ch rysa nthe- mate (Bioresmethrin) which is one of the more toxic chrysanthemate esters known to houseflies and mustard beetles, its toxicity being about 24 times that of allethrin to houseflies and 65 times that of allethrin to mustard beetles.

The following relative toxicities were recorded.

Relative Toxicity

Compound X Z R7/R3 Houseflies Mustard Beetles Bioresmethrin 100 100 1 H H H 2 5 2 H H Br 25 9 3 H CH3 H 0.3 0.2 4 H CH3 Br 2 2 5 H CZECH H N1 2 6 H CZECH Br 2 7 7 H CN H 4 4 8 H CH Br 9 10 9 CH3 H. H NT 1 10 CH3 H Br 2 9 11 CI H H NT 0.3 12 Cl H Br 1 3 NT = not tested Compounds of formula I may be formulated as the active compound or as one of the active compounds in pesticidal compositions as described in the Formulation Examples below.

Formulation 1 Oil-based liquid spray for household insects actiye compound 0.015% w/v 25% Pyrethrum Extract 0.25% Piperonyl butoxide 0.5 /O Antioxidant 0.1% Odourless light oil solvent e.g. xylene to make 100 vols.

Formulation 2 Water-based liquid spray concentrate for mosquito control active compound 0.25% w/v Piperonyl butoxide 1.0% Non-ionic emulsifier 0.25% Antioxidant 0.1% Water to make 100 vols.

This concentrate should be diluted e.g. 1:80 w/v with water, before spraying.

Formulation 3 Aerosol active compound 0.05% 25% Pyrethrum Extract 0.8% Piperonyl butoxide 1.5% Odourless petroleum distillate (b.p.

200-265") 17.338% Propellant, e.g. a mixture of equal quantities of trichloromonofluoromethane and dichlorodifluoromethane 80.0% Perfume 0.2% Antioxidant 0.1% Formulation 4 Mosquito coil active compound 0.25% Tabu powder (also known as pyrethrum marc) 30.0% Filler(s), e.g. wood flour, powdered leaves or nut shells 68.75% Brilliant Green (dyestuff) 0.5% n-Nitrophenol 0.5% Formulation 5 Emulsifiable concentrate active compound 1.5% w/v Non-ionic emulsifier 25.0% Xylene 73.4% Antioxidant 0.1% This concentrate may then be diluted at the rate of 30 mls. to 4 1/2 litres of water prior to use.

Formulation 6 General purpose powder for household, garden, livestock or grain storage use active compound 0.05% w/w Tropital (the synergist piperonyl-bis 2-[2'-n-butoxyethoxy]ethyl acetal 0.25% Antioxidant, e.g. butyl hydroxy toluene or butyl hydroxy anisole 0.03% Filler 99.67%

Claims (3)

1. A compound of the formula:

wherein X represents hydrogen, halogeno or an alkyl group and Z represents hydrogen, a methyl group or a cyano or ethynyl group.

2. A compound according to claim 1 wherein Z represents H or CN and X represents H, CH3 or CI.

3. A compound according to claim 1 hereinbefore specifically mentioned.