Preparation of alpha-cyano-phenoxybenzyl esters

Claim 2

A process for the preparation of an alpha-cyano-phenoxybenzyl ester of the formula: ##STR8## in which an acid halide of the formula: ##STR9## in which R is an optionally substituted cyclopropyl group or an optionally substituted benzyl group and X is fluorine, chlorine or bromine is reacted with an ester of an alpha-cyano-phenoxybenzyl alcohol of the formula: ##STR10## in which R 1 is a straight chain or branched chain alkyl group containing from 1 to 6 carbon atoms in the presence of an inert polar aprotic solvent and a transition metal alkoxide catalyst.

Claim 3

A process for the preparation of an alpha-cyano-phenoxybenzyl ester of the formula: ##STR11## in which an acid halide of the formula: ##STR12## in which R is (i) a cyclopropyl group of the formula ##STR13## in which R a and R b each is an alkyl group containing from 1 to 6 carbon atoms, or a halogen atom selected from flourine, chlorine or bromine, or R a is a hydrogen atom and R b is an alkenyl group containing from 2 to 6 carbon atoms optionally substituted with from 1 to 3 chlorine or bromine atoms, R c and R d each is an alkyl group containing from 1 to 6 carbon atoms, or R c is hydrogen and R d is R b , or R a and R b together or R c and R d together is an alkylene group containing from 2 to 6 carbon atoms; or R is (ii) a benzyl group of the formula ##STR14## in which Z is a halogen atom selected from flourine, chlorine or bromine or an alkoxy group containing from 1 to 4 carbon atoms and Y is a straight chain or branched chain alkyl group containing from 1 to 6 carbon atoms is reacted with an ester of an alpha-cyano-phenoxybenzyl alcohol of the formula: ##STR15## in which R 1 is a straight chain or branched chain alkyl group containing from 1 to 6 carbon atoms in the presence of an inert polar aprodic solvent and a transition metal alkoxide catalyst.

Claim 4

A process for the preparation of an alpha-cyano-phenoxybenzyl ester of the formula: ##STR11## in which an acid halide of the formula: ##STR12## in which R is (i) a cyclopropyl group of the formula ##STR13## in which R a and R b each is an alkyl group containing from 1 to 6 carbon atoms, or a halogen atom selected from flourine, chlorine or bromine, or R a is a hydrogen atom and R b is an alkenyl group containing from 2 to 6 carbon atoms optionally substituted with from 1 to 3 chlorine or bromine atoms, R c and R d each is an alkyl group containing from 1 to 6 carbon atoms, or R c is hydrogen and R d is R b , or R a and R b together or R c and R d together is an alkylene group containing from 2 to 6 carbon atoms; or R is (ii) a benzyl group of the formula ##STR14## in which Z is a halogen atom selected from flourine, chlorine or bromine or an alkoxy group containing from 1 to 4 carbon atoms and Y is a straight chain or branched chain alkyl group containing from 1 to 6 carbon atoms is reacted with an ester of an alpha-cyano-phenoxybenzyl alcohol of the formula: ##STR15## in which R 1 is a straight chain or branched chain alkyl group containing from 1 to 6 carbon atoms in the presence of an inert polar aprodic solvent and a transition metal alkoxide catalyst.

Claim 5

A process according to claim 2 wherein said solvent is isopropyl ether.

Claim 6

A process according to claim 2 wherein said solvent is diethyl ether.

Claim 7

A process according to claim 2 wherein said catalyst is titanium tetrabutoxide.

Claim 8

A process according to claim 2 wherein said process is carried out from a temperature of about 40° C. to about 100° C.

Claim 9

A process according to claim 1 wherein said phenoxybenzyl ester is an alpha-cyano-3-phenoxybenzyl ester of tetramethylcyclopropane carboxylic acid, dimethyl-dichlorylvinyl-cyclopropane carboxylic acid, dimethyl-dibromovinyl-cyclopropane carboxylic acid or 2-(4-chlorophenyl)-3-methylbutyric acid.