Copper-catalyzed O-arylation of phenols with diazonium salts

被引:7
|
作者
Fang, Xin [1 ]
Qi, Chengning [1 ]
Cao, Xiangqian [1 ]
Ren, Zhi-Gang [1 ]
Young, David James [2 ]
Li, Hong-Xi [1 ]
机构
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Jiangsu, Peoples R China
[2] Univ Elect Sci & Technol China, Glasgow Coll UESTC, Chengdu 611731, Peoples R China
基金
中国国家自然科学基金;
关键词
DIARYL ETHERS; PHOTOREDOX CATALYSIS; CROSS-COUPLINGS; ARYL HALIDES; ARENEDIAZONIUM; BOND; CHEMISTRY; STRATEGY; ACIDS; MILD;
D O I
10.1039/d3gc02541a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
It is well known that diazonium salts (ArN2+) react with phenols (Ar ' OH) to give aryl diazoethers or diazo compounds, but their cross-coupling to exclusively access diaryl ethers is challenging. Herein we disclose the Cu-catalyzed etherification of phenols with aryl diazonium salts at room temperature, yielding diaryl ethers in moderate to excellent yields. The advantages of this protocol are mild reaction conditions, availability of reactants, operational simplicity, high tolerance of other functional groups and easy work-up. Its application to the synthesis of complex biological molecules is demonstrated. The reaction proceeds through single-electron transfer, extrusion of nitrogen, oxidative addition, and reductive elimination to give diaryl ether products.
引用
收藏
页码:8068 / 8073
页数:6
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