Article ID Journal Published Year Pages File Type
10244398 Journal of Catalysis 2005 5 Pages PDF
Abstract
Cryptomelane-type manganese oxides octahedral molecular sieve (K-OMS-2) were used for the acid-catalyzed condensation of phenylhydroxylamine with aniline to produce 2-aminodiphenylamine. The H+-exchanged K-OMS-2 was found to be an efficient catalyst for this reaction. The reaction showed high selectivity (∼96%) for the ortho isomer of aminodiphenylamine compared with the para product. The effect of the amount of H+ exchange and temperature was investigated.
Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
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