Direct conversion of phenols into primary anilines with hydrazine catalyzed by palladium

被引:88
|
作者
Qiu, Zihang [1 ,2 ]
Lv, Leiyang [1 ,2 ]
Li, Jianbin [1 ,2 ]
Li, Chen-Chen [1 ,2 ]
Li, Chao-Jun [1 ,2 ]
机构
[1] McGill Univ, Dept Chem, 801 Sherbrooke St W, Montreal, PQ H3A 0B8, Canada
[2] McGill Univ, FQRNT Ctr Green Chem & Catalysis, 801 Sherbrooke St W, Montreal, PQ H3A 0B8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
AMMONIA; AMINES; LIGNIN; FUNCTIONALIZATION; 8-AMINOQUINOLINE; 4-AMINOPYRIDINE; AMINATION; MECHANISM; OXIMES; ACIDS;
D O I
10.1039/c9sc00595a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Primary anilines are essential building blocks to synthesize various pharmaceuticals, agrochemicals, pigments, electronic materials, and others. To date, the syntheses of primary anilines mostly rely on the reduction of nitroarenes or the transition-metal-catalyzed Ullmann, Buchwald-Hartwig and Chan-Lam cross-coupling reactions with ammonia, in which non-renewable petroleum-based chemicals are typically used as feedstocks via multiple step syntheses. A long-standing scientific challenge is to synthesize various primary anilines directly from renewable sources. Herein, we report a general method to directly convert a broad range of phenols into the corresponding primary anilines with the cheap and widely available hydrazine as both amine and hydride sources with simple Pd/C as the catalyst.
引用
收藏
页码:4775 / 4781
页数:7
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