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The hydrolysis of bromodifluoromethyltriphenylphosphonium bromide [1]
Authors:R.M. Flynn  R.G. Manning  R.M. Kessler  D.J. Burton  S.W. Hansen
Affiliation:National Institutes of Health, Department of Nuclear Medicine, Bethesda, Maryland 20205 U.S.A.;Department of Chemistry, University of Iowa, Iowa City, Iowa 52242 U.S.A.
Abstract:Hydrolysis of [Ph3P+CF2Br]Br? afforded a high yield of bromodifluoromethane and triphenylphosphine oxide. Hydrolysis in the presence of a radioactive isotope of bromine or sodium iodide gave unequivocal evidence that the mechanism for this reaction proceeds through a difluorocarbene intermediate.
Keywords:To whom correspondence should be addressed.
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