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Gomez, S., Peters, J.A. and Maschmeyer, T. (2002) The Reductive Amination of Aldehydes and Ketonesand the Hydrogenation of Nitriles: Mechanistic Aspects and Selectivity Control. Advanced Synthesis and Catalysis, 344, 1037- 1057.

has been cited by the following article:

• TITLE: Preparation of 2,5-Bis(Aminomethyl)Furan by Direct Reductive Amination of 2,5-Diformylfuran over Nickel-Raney Catalysts

  AUTHORS: Ngoc-Thuc Le, Areum Byun, Yohan Han, Kee-In Lee, Hyungrok Kim

  KEYWORDS: Reductive Amination, Primary Amine, 2, 5-Bis(Aminomethyl)Furan, 2, 5-Diformylfuran, Nickel Raney Catalyst

  JOURNAL NAME: Green and Sustainable Chemistry, Vol.5 No.3, August 5, 2015

  ABSTRACT: The direct reductive amination of 2,5-diformylfuran (DFF) with ammonia to 2,5-bis(aminomethyl)furan (BAF) was demonstrated, for the first time, over the commercial type Nickel-Raney and acid treated Nickel-Raney catalysts. The effects of reaction parameters such as reaction medium, temperature and hydrogen pressure were described. The acid treated Nickel-Raney catalyst exhibited the highest BAF yield in the THF-water mixed reaction medium. The relatively higher Ni0 species composition and larger surface area of the acid treated Nickel-Raney catalyst with specific reaction conditions contributed greatly to the BAF formation. The oligomeric species, such as furanic imine trimers and tetramers confirmed by MALDI-MS analysis were presented as the intermediates of DFF reductive amination.