p-Nitrosophenol chemistry. I. Etherification of p-nitrosophenol

JT Hays, EH De Butts, HL Young

Index: Hays,J.T. et al. Journal of Organic Chemistry, 1967 , vol. 32, p. 153 - 158

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Citation Number: 20

Abstract

Similarly, it reacts as a ketone with hydroxylamine to give quinone di~ xime.~'~ I n acetic acid, p-nitrosophenol reacts as a typical aromatic nitroso compound in yielding p- hydroxyazobenzene by reaction with aniline; 6 with strong sulfuric acid, it reacts with N, N- dimethylaniline to form an indoaniline.'While p-nitrosophenol has strongly acidic properties due to the activated phenolic group, 8 0-substituted p-nitrosophenols have not been ...