摘要
发展了一种在室温条件下,以PdBr2为催化剂,以[Bmim]Br/HBraq为溶剂,炔烃与烯丙醇进行交叉偶联反应的新方法,以中等及优良的产率(61%~93%)合成了溴代-1,4-二烯衍生物. 反应表现出较高的区域选择性和立体选择性. 催化体系可以循环使用4次,并且保持活性不变.
A Pd-catalyzed method was developed for cross-coupling reaction of a wide range of alkynes with allylic alcohol in ionic liquids. In the presence of PdBr2, [Bmim]Br and HBraq, the cross-coupling products can be obtained in moderate to good yields, and the reaction displayed high regio-and stereo-selectivities. The catalyst system could be recycled four times without loss of activity.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2013年第11期2407-2411,共5页
Chinese Journal of Organic Chemistry
基金
国家自然科学基金(No.21102047)
中央高校基金(No.2012ZM0037)资助项目~~
关键词
离子液体
钯催化
炔烃
烯丙醇
交叉偶联
ionic liquid palladium-catalyst alkyne allylic alcohol cross-coupling reaction