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Reductive Amination of Furanic Aldehydes in Aqueous Solution over Versatile Ni y AlO x Catalysts.


ABSTRACT: We disclose in this study a Ni6AlO x catalyst prepared by coprecipitation for the reductive amination of biomass-derived aldehydes and ketones in aqueous ammonia under mild reaction conditions. The catalyst exhibited 99% yield toward 5-aminomethyl-2-furylmethanol in the reaction of 5-hydroxymethyl furfural with ammonia at 100 °C for 6 h under 1 bar H2. The catalyst was further extended to the reductive amination of a library of aromatic and aliphatic aldehydes and ketones with a yield in the range 81-90% at optimized reaction conditions. Besides, 5-hydroxymethylfurfural could react with a library of primary and secondary amines with yields in the range 76-88%. The catalyst could be easily recycled and reused without apparent loss of activity in four consecutive runs.

SUBMITTER: Yuan H 

PROVIDER: S-EPMC6648111 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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Reductive Amination of Furanic Aldehydes in Aqueous Solution over Versatile Ni <sub><i>y</i></sub> AlO <sub><i>x</i></sub> Catalysts.

Yuan Hangkong H   Li Jerry-Peng JP   Su Fangzheng F   Yan Zhen Z   Kusema Bright T BT   Streiff Stéphane S   Huang Yongji Y   Pera-Titus Marc M   Shi Feng F  

ACS omega 20190201 2


We disclose in this study a Ni<sub>6</sub>AlO <sub><i>x</i></sub> catalyst prepared by coprecipitation for the reductive amination of biomass-derived aldehydes and ketones in aqueous ammonia under mild reaction conditions. The catalyst exhibited 99% yield toward 5-aminomethyl-2-furylmethanol in the reaction of 5-hydroxymethyl furfural with ammonia at 100 °C for 6 h under 1 bar H<sub>2</sub>. The catalyst was further extended to the reductive amination of a library of aromatic and aliphatic aldeh  ...[more]

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