Oxidation of primary alcohols to acyl fluorides using BrF 3
S Rozen, I Ben-David
Index: Rozen, Shlomo; Ben-David, Iris Journal of Fluorine Chemistry, 1996 , vol. 76, # 2 p. 145 - 147
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Citation Number: 29
Abstract
Aliphatic and alicyclic primary alcohols when treated with BrF3 were rapidly oxidized to the corresponding acyl fluorides. The reaction is of an ionic nature. The main by-product was found to be the symmetrical ester which originates from the reaction between the acyl fluoride and unreacted starting alcohol.
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