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Synthesis of Secondary Amines by Reductive Amination of Aldehydes with Nitroarenes over Supported Copper Catalysts in a Flow Reactor Full article

Journal Catalysis Communications
ISSN: 1566-7367 , E-ISSN: 1873-3905
Output data Year: 2017, Volume: 102, Pages: 108-113 Pages count : 6 DOI: 10.1016/j.catcom.2017.09.001
Tags Aldehyde, Continuous flow reactor, Molecular hydrogen, Nitroarene, One-pot reductive amination, Supported copper catalyst
Authors Nuzhdin Alexey L. 1 , Artiukha Ekaterina A. 1 , Bukhtiyarova Galina A. 1 , Derevyannikova Elizaveta A. 1,2 , Bukhtiyarov Valerii I. 1,2
Affiliations
1 Boreskov Institute of Catalysis SB RAS, Lavrentieva Ave. 5, Novosibirsk 630090, Russia
2 Novosibirsk State University, Pirogova Str. 2, Novosibirsk 630090, Russia

Funding (1)

1 Federal Agency for Scientific Organizations 0303-2016-0006 (V.44.1.6)

Abstract: Supported copper catalysts were investigated for the one-pot reductive amination of aldehydes with nitroarenes in a continuous flow reactor. This process is considered advantageous compared to current traditional methods, which present several drawbacks, such as toxicity of reducing or alkylation agent, lack of monoalkylation selectivity and large amounts of waste produced. Various secondary amines were synthesized in good to excellent yields in the reactions of aliphatic aldehydes with nitroarenes using molecular hydrogen as a reducing agent. It was found that the yield of secondary amine depends on the rate of formation of intermediate imine.
Cite: Nuzhdin A.L. , Artiukha E.A. , Bukhtiyarova G.A. , Derevyannikova E.A. , Bukhtiyarov V.I.
Synthesis of Secondary Amines by Reductive Amination of Aldehydes with Nitroarenes over Supported Copper Catalysts in a Flow Reactor
Catalysis Communications. 2017. V.102. P.108-113. DOI: 10.1016/j.catcom.2017.09.001 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Jun 20, 2017
Accepted: Sep 3, 2017
Published online: Sep 5, 2017
Published print: Dec 1, 2017
Identifiers:
Web of science: WOS:000413058800025
Scopus: 2-s2.0-85029178266
Elibrary: 31039549
Chemical Abstracts: 2017:1488910
Chemical Abstracts (print): 167:431173
OpenAlex: W2753150747
Citing:
DB Citing
Web of science 38
Scopus 40
Elibrary 35
OpenAlex 38
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