A Reusable Mesoporous Nickel Nanocomposite Catalyst for the Selective Hydrogenation of Nitroarenes in the Presence of Sensitive Functional Groups

The synthesis of aromatic amines from nitroarenes through hydrogenation is an industrially and academically important reaction. In addition, the employment of base metal catalysts in reactions that are preferentially mediated by rare noble metals is a desirable aim in catalysis and an attractive ele...

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Bibliographic Details
Published inChemCatChem Vol. 8; no. 15; pp. 2461 - 2465
Main Authors Hahn, Gabriela, Ewert, Julia-Katharina, Denner, Christine, Tilgner, Dominic, Kempe, Rhett
Format Journal Article
LanguageEnglish
Published Weinheim Blackwell Publishing Ltd 08.08.2016
Wiley Subscription Services, Inc
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Summary:The synthesis of aromatic amines from nitroarenes through hydrogenation is an industrially and academically important reaction. In addition, the employment of base metal catalysts in reactions that are preferentially mediated by rare noble metals is a desirable aim in catalysis and an attractive element‐conservation strategy. Especially appealing is the observation of novel selectivity patterns with such inexpensive metal catalysts. Herein, we report a novel mesostructured Ni nanocomposite catalyst. It is the first example of a reusable Ni catalyst that is able to hydrogenate nitroarenes selectively to anilines in the presence of highly sensitive functional groups such as C=C bonds and nitrile, aldehyde, and iodo substituents. Why so sensitive? A novel mesostructured Ni nanocomposite catalyst that is easy to synthesize and scale up is introduced. It is a reusable catalyst for the selective hydrogenation of nitroarenes to anilines. Highly hydrogenation‐sensitive groups such as olefins and aldehydes are tolerated.
Bibliography:ark:/67375/WNG-8HKMHV8Z-V
Deutsche Forschungsgemeinschaft - No. SFB 840, project B1
ArticleID:CCTC201600391
istex:EDD018872B6FB3E7E4EF2F332B11977EA5307A59
ISSN:1867-3880
1867-3899
DOI:10.1002/cctc.201600391