摘要
本文通过苊并咪唑氮杂环卡宾催化惰性C-S键的活化反应,成功实现了C-S/C-N偶联反应。经过条件优化后,可在温和条件下实现硫醚的高效转化,各种电子效应、位阻效应以及杂环底物均能很好地兼容,并以良好的产率得到相应的芳胺类化合物,为有机物脱硫奠定基础。
In this paper,the C-S/C-N coupling reaction was successfully realized by the activation of inert C-S bonds catalyzed by acenaphthoimidazolylidene palladium catalyst.After the optimization of reaction conditions,the efficient conversion of thioethers could be realized under mild conditions.Various substrates with different electronic effects,steric effects and heterocyclic substrates could be well tolerated in this catalytic system,and the corresponding aromatic amines could be obtained in good yields.This process would lay the foundation for the highly concerned desulfurization of organic compounds.
作者
申雅靓
朱海波
洪龙城
张超
Shen Yajing;Zhu Haibo;Hong Longcheng;Zhang Chao(Institute of(Bio)Pharmaceutical Research,Institute of Zhejiang University-Quzhou,Zhejiang,324003;School of Chemistry,Biology and Material Science,East China University of Technology,Jiangxi,330013)
出处
《当代化工研究》
2022年第19期36-38,共3页
Modern Chemical Research
基金
浙江大学衢州研究院科技计划项目“多孔有机金属材料制备及其在CO_(2)催化转化中的应用”(项目编号:IZQ2021KJ2010)
浙江大学衢州研究院科技计划项目“从木质素到药物活性分子的降解转化研究”(项目编号:IZQ2021KJ2019)
浙江大学衢州研究院科技计划项目“2,3-丁二醇选择性脱氢合成3-羟基丁酮高效Cu基催化剂研究及工艺开发”(项目编号:IZQ2021KJ2015)
浙江大学衢州研究院自主科研专项项目“氮杂环卡宾催化材料的制备及其在二氧化碳高效转化中的应用”(项目编号:IZQ2021RCZX027)。
关键词
氮杂环卡宾
钯
C-S键活化
偶联
N-heterocyclic carbene
palladium
activation of C-S bond
coupling