Issue 14, 1977

Synthesis of thioesters by reactions of carboxylic acids with tris(ethylthio)borane

Abstract

Thioesters are obtained in high yield by reactions of carboxylic acids with tris(ethylthio)borane in a refluxing solvent. The reaction pathway is complex, involving initial production of carboxylic anhydrides and oxybis(diacyloxy-boranes), which are separately attacked by liberated ethanethiol or the excess of tris(ethylthio)borane.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1977, 1672-1674

Synthesis of thioesters by reactions of carboxylic acids with tris(ethylthio)borane

A. Pelter, T. E. Levitt, K. Smith and A. Jones, J. Chem. Soc., Perkin Trans. 1, 1977, 1672 DOI: 10.1039/P19770001672

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