A convenient and mild synthetic route to aminoarenes by reduction of nitroarenes with activated nickel and hydrazine hydrate

Article abstract of DOI:10.1080/00397919708005010

Aminoarenes were obtained in excellent yields by reduction of corresponding nitroarenes with activated nickel powder and hydrazine hydrate. The nickel catalyst was prepared by the reduction of anhydrous nickelous chloride with Ultrasonically Dispersed Potassium.

Full text of DOI:10.1080/00397919708005010

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Convenient and Mild
Synthetic Route to
Aminoarenes by Reduction of
Nitroarenes with Activated
Nickel and Hydrazine Hydrate
Hongbin Li a , Rong Zhang a , Hui Wang a , Yi Pan a &
Yaozeng Shi a
a Department of Chemistry, Nanjing University,
Nanjing, 210093, P.R. China
Version of record first published: 22 Aug 2006.
To cite this article: Hongbin Li, Rong Zhang, Hui Wang, Yi Pan & Yaozeng Shi (1997): A
Convenient and Mild Synthetic Route to Aminoarenes by Reduction of Nitroarenes with
Activated Nickel and Hydrazine Hydrate, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 27:17, 3047-3052
To link to this article: http://dx.doi.org/10.1080/00397919708005010
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