Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sumitomo Chemical Co LtdfiledCriticalSumitomo Chemical Co Ltd
Priority to JP614480ApriorityCriticalpatent/JPS56103174A/en
Publication of JPS56103174ApublicationCriticalpatent/JPS56103174A/en
Publication of JPH0130830B2publicationCriticalpatent/JPH0130830B2/ja
Agricultural Chemicals And Associated Chemicals
(AREA)
Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms
(AREA)
Abstract
NEW MATERIAL:Optically active α-cyano-3-phenoxybenzyl 2-( 3, 4-methylenedioxyphenyl)-isovalerate.
USE: Insecticide or acaricide, which has some twice to four times activity of the racemic isomer.
PREPARATION: For example, a metal salt of S(+)-2-(3,4-methylenedioxy)isovaleric acid is made to react with an α-halogeno-3-phenoxyphenylacetonitrile to form the S(±) isomer in the acid side of a compound of the formula. Then, preferably the product is dissolved in a solvent of a lower alcohol and crystal seeds are inoculated to cause crystallization at -50W20°C. The crystals precipitated are removed to give the acid-side S(+) isomer of the formula rich in the exemplified compound.
COPYRIGHT: (C)1981,JPO&Japio
JP614480A1980-01-211980-01-21Optically active carboxylic ester, its preparation and insecticide and acaricide
GrantedJPS56103174A
(en)
Derivatives of 2,2-dimethyl-3-haloalkenyl-cyclopropane carboxylic acid esters with fluorinated-3-trifluoromethoxy benzyl alcohols and 5-(2-fluoro-1,3-benzodioxole)methanols,their preparation and their use as pesticides