ISSN:
0170-2041
Keywords:
Pyrethroids
;
Olefins, bis(trifluoromethyl)-substituted
;
Caronaldehydic acid methyl ester, hexafluoro-
;
Chrysanthemic acid, hexafluoro-
;
Chemistry
;
Organic Chemistry
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
Synthesis of cis-Configurated Bis(trifluoromethyl)pyrethroidstrans-2,2-Bis(trifluoromethyl)cyclopropanecarboxylates 2a, b are converted into the cis-diastereomers by base-catalyzed epimerization via the bicyclic lactones 3a, b. Dehydration of cis-2a and cleavage of the ester function leads to the fluorinated chrysanthemic acid 4b, which is converted into the pyrethroids 4d, e. cis-2b is oxidized by pyridinium chlorochromate to give methyl cis-3-formyl-2-2-bis(trifluoromethyl)-cyclopropanecarboxylate (hexafluorocaronaldehydic acid methyl ester) (5). This compound, which is very sensitive to isomerization, is converted into the pyrethroid esters 6a, b predominately retaining the cis configuration; however, by introducing the 2,2-dichlorovinyl side chain the trans diastereomer is obtained. The starting materials trans-2a, b are prepared by the reaction of aldehydes 9a, b with 2,2-dichlorohexafluoropropane and triphenylphosphine followed by cyclopropanization of the resulting 1,1-bis(trifluoromethyl)olefins 10a, b with (ethoxycarbonylmethylene)dimethylsulfurane (14).
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/jlac.1991199101175
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