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作 者:袁艳琴[1] 郭圣荣[1] 莫建军[1] 钱利[1] 石泽凤[1]
出 处:《有机化学》2012年第4期732-741,共10页Chinese Journal of Organic Chemistry
基 金:浙江省自然科学基金基金(No.Y407240);丽水学院重点科研(No.KZ20H03)资助项目~~
摘 要:在无金属催化剂的条件下,利用微波加热促进C—O,C—N和C—S交叉偶联反应.实验发现以DMSO为溶剂,t-BuOK为碱,利用微波加热,活化的氯代芳烃能与各类亲核试剂顺利反应,得到中等及优良的产率.A rapid and direct coupling reactions of various N/O/S nucleophilic reagents with aryl halides have been developed in good to high yields under microwave irradiation without a transition-metal catalyst.These reactions are a particularly powerful method for the coupling of electron-withdraw aryl halides with various nucleophilic reagents.A variety of products including aryl ethers,N-arylamides,and aryl thioethers were synthesized in good to excellent yields.
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