A general route for the synthesis of β,β-difluorocarboxylic acids

Or Cohen, Shlomo Rozen*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

A new method for the preparation of β,β-difluoro- (and other gem-difluoro) acids has been developed. It is based on the fact that 3-oxocarboxylic esters are easy to make and convert to the corresponding dithiane derivatives. These dithianes reacted with BrF3, a commercial, but rarely used reagent in organic chemistry, under very mild conditions to form the corresponding difluoroesters, which in turn could be quantitatively hydrolyzed to the free gem-difluoroacids.

Original languageEnglish
Pages (from-to)5362-5364
Number of pages3
JournalTetrahedron
Volume64
Issue number22
DOIs
StatePublished - 26 May 2008

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