2-(2,6-Dimethylphenylamino)-2-oxoacetic Acid as an Efficient Prompter for the Copper-Catalyzed Hydroxylation of Aryl Bromides

doi:10.6023/cjoc201206001

Chin. J. Org. Chem. ›› 2012, Vol. 32 ›› Issue (08): 1434-1438.DOI: 10.6023/cjoc201206001 Previous Articles Next Articles

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2-(2,6-二甲基苯胺基)-2-氧代乙酸促进的铜催化的芳基溴代物的羟基化

刘向前^a, 张慧^a, 蒋咏文^b

a 上海大学化学系上海 200444;
b 中国科学院上海有机化学研究所生命有机国家重点实验室上海 200032

收稿日期:2012-06-01 修回日期:2012-06-15 发布日期:2012-06-20
通讯作者: 张慧, 蒋咏文 E-mail:jiangyw@mail.sioc.ac.cn&yehao7171@163.com
基金资助:
国家自然科学基金(No. 20921091)资助项目.

2-(2,6-Dimethylphenylamino)-2-oxoacetic Acid as an Efficient Prompter for the Copper-Catalyzed Hydroxylation of Aryl Bromides

Liu Xiangqian^a, Zhang Hui^a, Jiang Yongwen^b

a Department of Chemistry, Shanghai University, Shanghai 200444;
b State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032

Received:2012-06-01 Revised:2012-06-15 Published:2012-06-20
Supported by:
Project supported by the National Natural Science Foundation of China (No. 20921091).

CuI/2-(2,6-dimethylphenylamino)-2-oxoacetic acid (DMPAO) as an efficient catalytic combination was used for the hydroxylation of aryl bromides. The catalyst loading is low to 2 mol% and substituted phenols could be prepared in wide assembly. In addition, by modifying the mixed solvent and base the symmetrical diaryl ethers could be synthesized conveniently from aryl bromides.

Key words: copper, Ullmann reaction, 2-(2,6-dimethylphenylamino)-2-oxoacetic acid, hydroxylation, phenol

Cite this article

Liu Xiangqian, Zhang Hui, Jiang Yongwen. 2-(2,6-Dimethylphenylamino)-2-oxoacetic Acid as an Efficient Prompter for the Copper-Catalyzed Hydroxylation of Aryl Bromides[J]. Chin. J. Org. Chem., 2012, 32(08): 1434-1438.

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2-(2,6-二甲基苯胺基)-2-氧代乙酸促进的铜催化的芳基溴代物的羟基化

2-(2,6-Dimethylphenylamino)-2-oxoacetic Acid as an Efficient Prompter for the Copper-Catalyzed Hydroxylation of Aryl Bromides

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