The ortho-substituted N,N-diacetylaniline as a selective acetylating reagent.

被引:38
作者
Murakami, Y
Kondo, K
Miki, K
Akiyama, Y
Watanabe, T
Yokoyama, Y
机构
[1] School of Pharmaceutical Sciences, Toho University, Funabashi, Chiba 274
关键词
D O I
10.1016/S0040-4039(97)00745-4
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Selective acetylation of the less hindered amino group in the presence of the more hindered amino group with the use of 2-trifluoromethyl-N,N-diacetylaniline 2c is described. This acetylation with 2c yielded the corresponding less hindered monoacetamide exclusively, simply, conveniently, and in good yields. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:3751 / 3754
页数:4
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