作者:Dietmar Seyferth、David C. Mueller
DOI:10.1016/s0022-328x(00)88013-4
日期:1971.5
Phenyl(1,1-dichloroethyl)mercury has been prepared via 1,1-dichloroethyllithium and evaluated as a potential CH3CCl transfer agent. Although this mercurial reacted with triethylsilane to give Et3SiCHClCH3 (35%) and with allyltrimethylsilane to give 1-chloro-1-methyl-2-(trimethylsilylmethyl)cyclopropane (31%), its principal mode of reaction involved elimination of hydrogen chloride. The products resulting
苯基(1,1-二氯乙基)汞已通过1,1-二氯乙基锂制备,并被评估为潜在的CH 3 CCl转移剂。尽管该汞与三乙基硅烷反应生成Et 3 SiCHClCH 3(35%),与烯丙基三甲基硅烷反应生成1-氯-1-甲基-2-(三甲基甲硅烷基甲基)环丙烷(31%),但其主要反应方式涉及消除氯化氢。 。从这种消除产生的产物是苯(从PhHg键盐酸裂解)和含有伴随形成HgCClCH引入的汞化合物2部分。讨论了这种意外反应的可能原因。