One pot catalytic NO2 reduction, ring hydrogenation, and N-alkylation from nitroarenes to generate alicyclic amines using Ru/C-NaNO2
- Authors
- Oh, Seung Geun; Mishra, Vivek; Cho, Jin Ku; Kim, Baek-Jin; Kim, Hoon Sik; Suh, Young-Woong; Lee, Hyunjoo; Park, Ho Seok; Kim, 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
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.