作者:F.R. Stermitz、D.W. Neiswander
DOI:10.1016/0040-4020(75)80065-2
日期:1975.1
Reaction of phenylnitromethane with acetic anhydride/sodium acetate at 80–85° produces N-benzoyl-N,O-diacetylhydroxylamine, which can be isolated in 30% yield. This compound was proposed previously as an intermediate in a similar reaction which had yielded only benzoic anhydride, triacetylhydroxylamine and acetanilide.
苯硝基甲烷与乙酸酐/乙酸钠在80–85°下反应生成N-苯甲酰基-N,O-二乙酰基羟胺,可以将其分离,产率为30%。该化合物先前被提议作为类似反应的中间体,该反应仅产生苯甲酸酐,三乙酰基羟胺和对乙酰苯胺。