CARBON–SILICON BOND CLEAVAGE OF ORGANOTRIALKOXYSILANES AND ORGANOSILATRANES WITH<i>m</i>-CHLOROPERBENZOIC ACID AND<i>N</i>-BROMOSUCCINIMIDE. NEW ROUTE TO PHENOLS, PRIMARY ALCOHOLS AND BROMIDES
作者:Akira Hosomi、Susumu Iijima、Hideki Sakurai
DOI:10.1246/cl.1981.243
日期:1981.2.5
Alkyl- and aryltriethoxysilanes undergo oxidative carbon–silicon bond cleavage smoothly with m-chloroperbenzoic acid (MCPBA) to afford the corresponding alcohols. Silatranes similarly gave alcohols and bromides with MCPBA and N-bromosuccinimide, respectively.
烷基和芳基三乙氧基硅烷能够顺利地通过间氯过氧苯甲酸(m-氯过氧苯甲酸)进行氧化碳硅键断裂,得到相应的醇。类似地,硅拉烷分别与m-氯过氧苯甲酸和N-溴代丁二酰亚胺反应,分别得到醇和溴化物。