A STUDY OF SOME NEW HYDROXAMIC ACIDS OF HYDROXY AND ALKOXY FATTY ACIDS1

LW Jones, DH Powers

Index: Jones; Powers Journal of the American Chemical Society, 1924 , vol. 46, p. 2530

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Citation Number: 5

Abstract

The final rearrangement products depend upon experimental conditions. Thus, when an alkali salt of an acyl ester of a monohydroxamic acid, RCON (K) OCOR', is heated alone, the isocyanate may be isolated; but when it is heated with mater, the isocyanate generally reacts to give an amine or a disubstituted urea, and when alcohol is employed as a solvent, a urethan is usually formed.

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