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  4. Catalysis in flow: nickel-catalyzed synthesis of primary amines from alcohols and NH3
 
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Catalysis in flow: nickel-catalyzed synthesis of primary amines from alcohols and NH3
File(s)
acceptedmanuscript.pdf (444.34 KB)
Accepted version
Author(s)
Keung Leung, AY
Hellgardt, K
Leung, Andrew
Hii, KM
Type
Journal Article
Abstract
A highly selective synthesis of primary amines from alcohols and NH3 was achieved on using a commercially available Ni catalyst, without adding H2. Using a continuous flow reaction platform, the amination of aliphatic alcohols can be achieved in good yields and selectivities, as the accumulation of water byproduct can be removed. Competitive formation of the nitrile side-product was suppressed when the catalyst was prereduced. Modes of catalyst deactivation were also briefly examined.
Date Issued
2018-03-05
Date Acceptance
2018-02-19
Citation
ACS Sustainable Chemistry and Engineering, 2018, 6 (4), pp.5479-5484
URI
http://hdl.handle.net/10044/1/57850
DOI
https://www.dx.doi.org/10.1021/acssuschemeng.8b00338
ISSN
2168-0485
Publisher
American Chemical Society
Start Page
5479
End Page
5484
Journal / Book Title
ACS Sustainable Chemistry and Engineering
Volume
6
Issue
4
Copyright Statement
© 2018 American Chemical Society.
Subjects
Science & Technology
Physical Sciences
Technology
Chemistry, Multidisciplinary
GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY
Engineering, Chemical
Chemistry
Science & Technology - Other Topics
Engineering
Atom-efficient
Continuous flow process
Hydrogen-borrowing
Nickel
Selective
Primary amines
N-ALKYLATION
HYDROXIDE CATALYSTS
SECONDARY-AMINES
DIRECT AMINATION
AMMONIA
FORMULATIONS
COMPLEXES
EFFICIENT
Publication Status
Published
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