Process for the manufacture of R-(+)-2-(4-(4-cyano-2-fluorophenoxy)phenoxy)propionic acid esters
View Patent ↗Cyhalofop esters are prepared by coupling 2-(4-hydroxyphenoxy)-propionic acid with 3,4-difluorobenzonitrile with base in a polar aprotic solvent (optionally including a phase-transfer catalyst), alkylating with alkyl halide, removing the polar aprotic solvent (optionally using cyhalofop ester as a flux), removing salt by aqueous extraction of molten cyhalofop ester without a solvent, and removing residual water by heating under reduced pressure.
1. An improved process for the manufacture of R-(+)-2-(4-(4-cyano-2-fluorophenoxy)phenoxy)propionate esters of the formula
wherein R represents C 1 -C 8 alkyl
which comprises:
a) forming a di (alkali metal salt) of R-(+)-2-(4-hydroxyphenoxy)propionic acid by contacting R-(+)-2-(4-hydroxyphenoxy)propionic acid in a polar aprotic solvent, having a dipole moment of at least 2 or dielectric constant of at least 7 and having a normal boiling point of less than 175° C., with at least two equivalents of alkali metal carbonate;
b) forming R-(+)-2-(4-(4-cyano-2-fluorophenoxy)phenoxy)propionic acid alkali metal salt by coupling the di (alkali metal salt) of R-(+)-2-(4-hydroxyphenoxy)propionic acid reaction mixture of step a) with 3,4-difluorobenzonitrile in the presence of a phase-transfer catalyst at a temperature from about 120° C. to about 150° C. in a sealed pressure vessel;
c) forming R-(+)-2-(4-(4-cyano-2-fluorophenoxy)phenoxy)propionic acid alkyl ester by alkylating the R-(+)-2-4-(4-cyano-2-fluorophenoxy)phenoxy)propionic acid alkali metal salt reaction mixture of step b) with an alkyl halide;
d) removing and recovering the polar aprotic solvent either by adding previously prepared, dry, molten R-(+)-2-(4-(4-cyano-2-fluorophenoxy)phenoxy)propionic acid alkyl ester to the reaction mixture of step c) and by distilling the polar aprotic solvent from the mixture, or by distilling the polar aprotic solvent from the mixture with agitation;
e) removing salt from the distillation bottoms of step d) by extracting the distillation bottoms with warm water and separating the aqueous brine from the organic layer; and
f) removing low boiling components such as water and unreacted 3,4-difluorobenzonitrile by distilling the organic layer from step e) under reduced pressure.