摘要
以苯硫酚为还原剂,在绿色溶剂、室温下将α,α,α-三溴甲基酮类化合物还原成α,α-二溴甲基酮类化合物.此反应适用于芳香族、脂肪族和杂环类α,α,α-三溴甲基酮类化合物,产率高达97%.进一步的机理研究表明,该反应是自由基反应.
α,α-Dibromomethyl ketones were synthesized with high yields through a thiophenol-promoted reduction of α,α,α-tribromomethyl ketones under mild conditions within one hour. A further mechanistic study showed that the reaction proceeded via a radical process. This is an example that uses thiophenol as the radical stimulator in the reduction of multi-halogenated compounds.
作者
杨莹
哈斯木江·巴拉提
阿布都热西提·阿布力克木
Yang Ying;Balati Hasimujiang;Abulikemu Abudu Rexit(Department of Chemistry,Xinjiang Normal University,Urumqi 830054)
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2019年第3期727-733,共7页
Chinese Journal of Organic Chemistry
基金
Project supported by the National Natural Science Foundation of China(No.21662035)~~