摘要
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.
Reaction of ketones with 1-butyl-3-methylimidazolium tribromide ([Bmim]Br3) under sol- vent-free conditions at room temperature, selectively gave the corresponding a-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.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2006年第2期236-238,共3页
Chinese Journal of Organic Chemistry
基金
江西省自然科学基金(No.0520001)
江西省教育厅科技资助项目.