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有机化学
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有机化学 ›› 2006, Vol. 26 ›› Issue (02): 236-238. 上一篇    下一篇

研究简报

[Bmim]Br3对酮的选择性单溴化反应

张胜建1，乐长高*,2   

  1. (1浙江大学宁波理工学院 宁波 315100)
    (2东华理工学院应用化学系 抚州 344000)
  • 收稿日期:2005-04-11 修回日期:2005-08-17 发布日期:2006-01-21
  • 通讯作者: 乐长高

Selective α-Monobromination of Ketones with [Bmim]Br3

ZHANG Sheng-Jian1,LE Zhang-Gao*,2   

  1. (1 Ningbo Institute of Technology, Zhejiang University, Ningbo 315100)
    (2 Department of Applied Chemistry, East China Institute of Technology, Fuzhou 344000)
  • Received:2005-04-11 Revised:2005-08-17 Published:2006-01-21
  • Contact: LE Zhang-Gao

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2017

在无溶剂和室温条件下, 三溴化1-丁基-3-甲基咪唑([Bmim]Br3)选择性地与酮反应, 以90%～96%的产率生成相应的α-溴代酮. 该方法反应条件温和、产率高、选择性好、环境友好.

关键词: 脂肪酮, 离子液体, 溴化, 三溴化1-丁基-3-甲基咪唑

Reaction of ketones with 1-butyl-3-methylimidazolium tribromide ([Bmim]Br3) under solvent-free conditions at room temperature, selectively gave the corre-sponding α-bromoketones with 90%～96% yields. Compared to the known report, this method has the advantages of mild reaction condition, good yields, high selectivity and more environmental benignity.

Key words: ionic liquid, alkanone, 1-butyl-3-methylimidazolium tribromide, bromination