One pot catalytic NO2 reduction, ring hydrogenation, and N-alkylation from nitroarenes to generate alicyclic amines using Ru/C-NaNO2

Authors
Oh, Seung GeunMishra, VivekCho, Jin KuKim, Baek-JinKim, Hoon SikSuh, Young-WoongLee, HyunjooPark, Ho SeokKim, Yong Jin
Issue Date
2014-01-05
Publisher
ELSEVIER SCIENCE BV
Citation
CATALYSIS COMMUNICATIONS, v.43, pp.79 - 83
Abstract
A report to produce alicyclic amines and subsequent N-alkylation with alcohols using Ru/C-NaNO2 catalyzed facile transformation of nitrobenzene was investigated. Effects of solvent, temperature, pressure, reaction time, and molar-ratio of substrate/catalyst on product composition were also studied. These mechanistic studies explain that nitrobenzene undergoes hydrogenation reaction in the following order; -NO2 reduction to -NH2, aromatic ring-hydrogenation to alicyclic, and from the reaction of alcohol to give N-alkylated amines. This investigation shed lights on possible application to polyurethane chemistry since these amines are used as important precursors for diisocyanates. (C) 2013 Elsevier B.V. All rights reserved.
Keywords
METAL CATALYSTS; CARBON-DIOXIDE; ANILINE; NITROBENZENE; ALCOHOLS; CYCLOHEXYLAMINE; COMPLEX; WATER; METAL CATALYSTS; CARBON-DIOXIDE; ANILINE; NITROBENZENE; ALCOHOLS; CYCLOHEXYLAMINE; COMPLEX; WATER; Hydrogenation; Nitrobenzene; Cyclohexylamine; Ruthenium catalyst
ISSN
1566-7367
URI
https://pubs.kist.re.kr/handle/201004/127230
DOI
10.1016/j.catcom.2013.09.012
Appears in Collections:
KIST Article > 2014
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE