Copper(I)-Catalyzed N-Arylation of N1,N3-Dibenzylmalonamide and N1,N3-Dibutylmalonamide Followed by Cleavage of the Malonyl Group with Aryl Halides Under Ligand-Free Conditions

被引:2
|
作者
Zheng, W. J. [1 ]
Xu, W. F. [1 ]
Shi, C. X. [2 ]
Ren, F. B. [1 ,3 ]
Lu, X. L. [1 ]
Zhou, Y. F. [1 ,3 ]
机构
[1] China Jiliang Univ, Coll Life Sci, Zhejiang Prov Key Lab Biometrol & Inspect & Quara, Hangzhou 310018, Zhejiang, Peoples R China
[2] Shanghai Univ, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China
[3] Zhejiang Apeloa Med Technol Co Ltd, Dongyang 322118, Peoples R China
关键词
Copper; Cleavage; Cross-coupling; N-1; N-3-Dibenzylmalonamide; N-3-Ditutylmalonamide; CROSS-COUPLING REACTIONS; CATALYZED AMINATION; AROMATIC AMINATION; ALIPHATIC-AMINES; C-C; COPPER; PALLADIUM; IODIDES; BROMIDES; BOND;
D O I
10.14233/ajchem.2013.13614
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We primarily developed a practical and convenient protocol to synthesize of aromatic amines based on CuI-catalyzed N-arylation of N-1,N-3-dibenzylmalonamide and N-1,N-3-dibutylmalonamide followed by cleavage of the malonyl group with aryl halides under ligand-free conditions giving good yields.
引用
收藏
页码:1117 / 1122
页数:6
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