催化学报 ›› 2007, Vol. 28 ›› Issue (6): 495-497.

• 研究快讯 • 上一篇    下一篇

2-硒代咪唑类化合物催化CO与胺的羰基化反应

李鹏1,2,王小芳1,原晓华1,王树东1,陆世维1   

  1. 1 中国科学院大连化学物理研究所国家催化工程中心, 辽宁大连 116011; 2 中国科学院研究生院, 北京 100049
  • 收稿日期:2007-06-25 出版日期:2007-06-25 发布日期:2011-05-28

Carbonylation of Amines with CO Catalyzed by Imidazole-2-selone

LI Peng1,2, WANG Xiaofang1, YUAN Xiaohua1, WANG Shudong1, LU Shiwei1*   

  1. 1 National Engineering Research Center for Catalysis, Dalian Institute of Chemical Physics, The Chinese Academy of Sciences, Dalian 116011, Liaoning, China; 2 Graduate University of Chinese Academy of Sciences, Beijing 100049, China
  • Received:2007-06-25 Online:2007-06-25 Published:2011-05-28

摘要: 首次研究了2-硒代咪唑类化合物催化的一氧化碳对胺的羰基化生成对称脲或口恶唑啉-2-酮的反应,目标产物收率中等到良好. 与传统的单质硒催化的羰基化反应相比,新催化体系有效避免了有恶臭气味的含硒化合物的产生.

关键词: 3-二烷基-2-硒代咪唑, 硒, 一氧化碳, 胺, 羰基化, 脲, 口恶唑啉-2-酮

Abstract: The1,3-dialkylimidazole-2-selones-catalyzedoxidative carbonylation of organic amines and ethanolamine with carbon monoxide to ureas and2-oxazolidinonewas investigated. Moderate to good product yields were obtained. Odour existing in elemental selenium-catalyzed carbonylation reactions can be avoided in this catalytic system.Key words:1,3-dialkylimidazoleselone;selenium; carbon monoxide; amine; carbonylation; urea; 2-oxazolidinone

Key words: 3-dialkylimidazoleselone, selenium, carbon monoxide, amine, carbonylation, urea, 2-oxazolidinone