摘要
以二苯二硫醚为硫源,在无强碱和配体的条件下,通过碘化亚铜催化促进S—S键断裂,再与苯并五元杂环化合物反应生成了芳基硫醚,采用1H NMR和13C NMR对目标化合物进行了表征,并确定了最佳反应条件.在苯并五元杂环化合物和二苯二硫醚的物质的量比为2∶1,催化剂Cu I用量为10 mol%,溶剂为二甲基亚砜(DMSO),反应温度110℃,时间12 h时,产率达到89.9%.同时,通过高效液相色谱(HLPC)进行跟踪监测,对该反应的机理进行了探讨.
In this study, the direct copper-catalyzed C--S coupling reaction of heterocyclic compounds with diphenyl disul- fide, without the existence of ligands and alkalis, has been developed. It showed that the yield of target product was 89.9% when the reaction was carried out at 110 ℃, the reaction time was 12 h, dimethylsulfoxide (DMSO) was used as solvents, and the molar ratio of heterocyclic compound to biphenyl disulfide was 2 : 1. The structures of the target products were confirmed with 1H NMR and 13C NMR. The effects of various conditions on the reaction were investigated by high performance liquid chromatography (HPLC) analysis and its reaction mechanism was discussed.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2015年第4期905-909,共5页
Chinese Journal of Organic Chemistry
基金
山西省科技基础条件平台建设(No.2013091026)
山西大学本科生科研训练(No.2014013)资助项目~~