The Carboaryloxy Radical in the Migration of Acyl from Nitrogen to Oxygen in Ortho Aminophenol Derivatives

Authors

L. Chas Raiford, State University of IowaFollow
G. O. Inman, State University of Iowa

Document Type

Research

Abstract

It has been shown, in general, that only one acetyl-benzoyl derivative of ortho aminophenols can be prepared, regardless of the order in which the acyl groups are introduced, and that in this product the benzoyl radical is always found attached to nitrogen. In the recent study of mixed diocyl derivatives of ortho aminophenols in which one of the radicals was the carboaryloxy group, attempts to determine the structure by means of hydrolysis with alkali caused the formation of a carbonylaminophenol.

Publication Date

1933

Journal Title

Proceedings of the Iowa Academy of Science

Volume

40

Issue

1

First Page

109

Last Page

109

Copyright

©1933 Iowa Academy of Science, Inc.

Language

en

File Format

application/pdf

Recommended Citation

Raiford, L. Chas and Inman, G. O. (1933) "The Carboaryloxy Radical in the Migration of Acyl from Nitrogen to Oxygen in Ortho Aminophenol Derivatives," Proceedings of the Iowa Academy of Science, 40(1), 109-109.
Available at: https://scholarworks.uni.edu/pias/vol40/iss1/47