Bamberger Rearrangement of N-Arylhydroxylamine to p-Aminophenol in a CO2

Bamberger Rearrangement of N-Arylhydroxylamine to p-Aminophenol in a CO2–H2O System

Published:2014-05-12 Issue:20 Volume:53 Page:8372-8375
ISSN:0888-5885
Container-title:Industrial & Engineering Chemistry Research
language:en
Short-container-title:Ind. Eng. Chem. Res.

Author:

Liu Shijuan¹,Hao Yuanping²,Jiang Jingyang²

Affiliation:

1. College of Chemistry, Key Laboratory of Preparation and Application of Environmental Friendly Materials of Ministry of Education, Jilin Normal University; Siping 136000 China

2. College of Chemical Engineering, State Key Laboratory of Fine Chemicals, Dalian University of Technology; Dalian 116024 China

Publisher

American Chemical Society (ACS)

Subject

Industrial and Manufacturing Engineering,General Chemical Engineering,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ie500864p

Reference28 articles.

1. Thomas, J. D.; Cedar, H.Method for preparing p-aminophenol. US 4264529, 1981.

2. Lain-tze, L.; Chen, M. H.; Yao, C. N.Process for manufacturing p-aminophenol. US 4885389, 1989.

3. Control of Competing Hydrogenation of Phenylhydroxylamine to Aniline in a Single-Step Hydrogenation of Nitrobenzene to p-Aminophenol

4. Ueber das Phenylhydroxylamin

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