CoPc/Cu(OAc)2-catalyzed N-arylation of amines with arylhydrazines leading to N-aryl amines

被引:13
|
作者
Sun, Wang-Bin [1 ]
Zhang, Pei-Zhi [1 ]
Jiang, Tao [1 ]
Li, Cheng-Kun [1 ]
An, Li-Tao [2 ]
Shoberu, Adedamola [1 ]
Zou, Jian-Ping [1 ,3 ]
机构
[1] Soochow Univ, Coll Chem & Chem Engn, Key Lab Organ Synth Jiangsu Prov, 199 Renai St, Suzhou 215123, Jiangsu, Peoples R China
[2] Huaiyin Normal Univ, Coll Chem & Chem Engn, 111 West Changjiang Rd, Huaian 223300, Jiangsu, Peoples R China
[3] Chinese Acad Sci, Key Lab Synthet Chem Nat Subst, Shanghai Inst Organ Chem, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
Arylation; Amine; CoPc; Catalysis; PALLADIUM-CATALYZED AMINATION; C-H AMINATION; CROSS-COUPLING REACTIONS; RADICAL ARYLATION; BOND FORMATION; ALIPHATIC-AMINES; ARYLBORONIC ACIDS; ANILINES; COPPER; DERIVATIVES;
D O I
10.1016/j.tet.2016.08.058
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The N-arylation of amines with arylhydrazines has been developed, achieving the selective cross coupling of aryl radicals with amines to form N-aryl amines. The reaction uses air as an oxidant, CoPc and Cu(OAc)(2) as catalysts. The reaction proceeds under mild conditions in air through a relay process, arylhydrazines are oxidized to aryldiazenes by CoPc, further oxidized to aryl radicals by air (O-2), which are trapped by Cu(OAc)(2)-amine complex, followed by reduction-elimination reaction to form N-aryl amines. Arylamines and arylhydrazines give the highest yields, but N-aryl-N-alkylamines and N-alkyl amines can be used as well. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6477 / 6483
页数:7
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