摘要
由烯烃经一氯硼烷甲硫醚(H2BCl·SMe2)硼氢化和甲醇解制得的二烷基硼酸甲酯6,在50%NaOH和相转移催化剂(TEBA)存在下与氯仿反应,继之氧化,获得了相应的二烷基酮1,二环烷基酮2和3以及脂环酮4.考查了各种参数对反应的影响.讨论了反应机理,为从烯烃出发合成各种类型的酮提供了一条简便新途径.
The methyl dialkylborinates, prepared from hydroboration of alkenes with monochloroborane-dimethyl sulfide and then methanolysis,react with 50% NaOH and chloroform under phase transfer conditions,followed by oxidation to give the corresponding dialkyl ketones 1,dicycloalkyl ketones 2 and 3, and alicyclic ketone 4. The influence of various reaction parameters on the reaction was examined and the reaction mechanism was also discussed to provide a new convenient route for synthesis of various ketones from alkenes.
出处
《武汉大学学报(自然科学版)》
CSCD
1995年第6期702-706,共5页
Journal of Wuhan University(Natural Science Edition)
基金
国家自然科学基金
关键词
酮
合成
二烷基硼酸甲酯
相转移反应
氯仿
organoborates,phase transfer catalysis,dichlorocarbene,insertion reaction,synthesis of ketones