Electrohydrogenation of Nitriles with Amines by Cobalt Catalysis

被引:4
|
作者
Wang, Tiantian [1 ]
He, Fangfang [1 ]
Jiang, Wei [1 ]
Liu, Jie [1 ,2 ]
机构
[1] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Peoples R China
[2] Hunan Univ, Greater Bay Area Inst Innovat, Guangzhou 511300, Guangdong, Peoples R China
关键词
Cobalt Catalysis; Hydrogenation; Nitriles; Organic Electrosynthesis; Reductive Amination; TRANSFER HYDROGENATION; RUTHENIUM HYDRIDE; SECONDARY-AMINES; DEUTERATION; REDUCTION; ELECTROREDUCTION; EVOLUTION; ALKENES; WATER;
D O I
10.1002/anie.202316140
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Catalytic hydrogenation of nitriles represents an efficient and sustainable one-step synthesis of valuable bulk and fine chemicals. We report herein a molecular cobalt electrocatalyst for selective hydrogenative coupling of nitriles with amines using protons as the hydrogen source. The key to success for this reductive reaction is the use of an electrocatalytic approach for efficient cobalt-hydride generation through a sequence of cathodic reduction and protonation. As only electrons (e-) and protons (H+) as the redox equivalent and hydrogen source, this general electrohydrogenation protocol is showcased by highly selective and straightforward synthesis of various functionalized and structurally diverse amines, as well as deuterium isotope labeling applications. Mechanistic studies reveal that the electrogenerated cobalt-hydride transfer to nitrile process is the rate-determining step. Reported herein is a mild and efficient electrocatalytic method for earth-abundant cobalt hydride generation through a sequence of cathodic reduction and protonation. The application of this molecular cobalt catalyst allows for electroreductive amination of nitriles to produce various secondary and tertiary amines, as well as deuterium isotope labeling applications from readily available deuterium source.image
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页数:9
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