Selective Hydrogenation of Nitriles to Primary Amines Catalyzed by a Polysilane/SiO2-Supported Palladium Catalyst under Continuous-Flow Conditions

被引:47
|
作者
Saito, Yuki [1 ]
Ishitani, Haruro [2 ]
Ueno, Masaharu [1 ]
Kobayashi, Shu [1 ,2 ]
机构
[1] Univ Tokyo, Sch Sci, Dept Chem, Bunkyo Ku, Tokyo 1130033, Japan
[2] Univ Tokyo, Grad Sch Sci, Green & Sustainable Chem Cooperat Lab, Bunkyo Ku, Tokyo 1130033, Japan
来源
CHEMISTRYOPEN | 2017年 / 6卷 / 02期
关键词
continuous flow; fine chemical synthesis; heterogeneous catalysis; hydrogenation; nitriles; PINCER COMPLEX; SILYLATIVE REDUCTION; SUPPORTED PALLADIUM; NITRO-COMPOUNDS; CHEMISTRY; AMINATION; BENZONITRILE; ALDEHYDES; IMINES; PHASE;
D O I
10.1002/open.201600166
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrogenation of nitriles to primary amines with heterogeneous catalysts under liquid-phase continuous-flow conditions is described. Newly developed polysilane/SiO2-supported Pd was found to be an effective catalyst and various nitriles were converted into primary amine salts in almost quantitative yields under mild reaction conditions. Interestingly, a complex mixture was obtained under batch conditions. Lifetime experiments showed that this catalyst remained active for more than 300h (TON10000) without loss of selectivity and no metal leaching from the catalyst occurred. By using this continuous-flow hydrogenation, synthesis of venlafaxine, an antidepressant drug, has been accomplished.
引用
收藏
页码:211 / 215
页数:5
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