催化学报 ›› 2006, Vol. 27 ›› Issue (12): 1051-1052.

• 研究快讯 • 上一篇    下一篇

NiCl2·6H2O催化芳基硼酸的自身偶联反应

刘谷雨,杜巧玲,谢俊杰,张恺黎,陶晓春   

  1. 华东理工大学金属有机化学研究室, 上海200237
  • 收稿日期:2006-12-25 出版日期:2006-12-25 发布日期:2006-12-25

NiCl2•6H2O-Catalyzed Homocoupling of Arylboronic Acids

LIU Guyu, DU Qiaoling, XIE Junjie, ZHANG Kaili, TAO Xiaochun*   

  1. Laboratory of Organometallic Chemistry, East China University of Science and Technology, Shanghai 200237, China
  • Received:2006-12-25 Online:2006-12-25 Published:2006-12-25

摘要: 通过筛选一系列有机溶剂,发现在吡啶中,以碳酸钾作碱,价廉易得的NiCl2·6H2O能催化芳基硼酸发生自身偶联反应生成对称的联芳烃,该反应收率较高,并可暴露在空气中进行.

关键词: 二氯化镍, 芳基硼酸, 自身偶联, 吡啶

Abstract: By screening different organic solvents, it was found that NiCl2•6H2O can catalyze the homocoupling of arylboronic acids using K2CO3 as the base in pyridine to produce symmetrical biaryls in good yield. This reaction can be carried out with exposure to air.

Key words: nickel chloride, arylboronic acid, homocoupling, pyridine