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通过双功能催化剂上5-(羟甲基)糠醛与NH的催化胺化反应高度选择性合成2,5-双(氨甲基)呋喃。

Highly selective synthesis of 2,5-bis(aminomethyl)furan catalytic amination of 5-(hydroxymethyl)furfural with NH over a bifunctional catalyst.

作者信息

Yuan Hangkong, Kusema Bright T, Yan Zhen, Streiff Stéphane, Shi Feng

机构信息

State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics (LICP), Chinese Academy of Sciences Lanzhou 730000 China

Eco-Efficient Products and Processes Laboratory (E2P2L), UMI 3464 CNRS-Solvay 3966 Jin Du Road, Xin Zhuang Ind. Zone 201108 Shanghai China

出版信息

RSC Adv. 2019 Nov 27;9(66):38877-38881. doi: 10.1039/c9ra08560b. eCollection 2019 Nov 25.

Abstract

The development of facile protocols for the selective synthesis of biomass-derived diamine is a highly desirable pursuit in the field of heterogeneous catalysis. Herein, a simple and highly efficient bi-functional CuNiAlO catalyst was developed for the one pot transformation of 5-(hydroxymethyl)furfural (5-HMF) into 2,5-bis(aminomethyl)furan (BAF) using a two-stage reaction process. CuNiAlO was found to be the most effective catalyst for this reaction, affording BAF in 85.9% yield. Our results could promote controllable conversion and utilization of biomass resource.

摘要

开发用于选择性合成生物质衍生二胺的简便方法是多相催化领域非常值得追求的目标。在此,开发了一种简单高效的双功能CuNiAlO催化剂,用于通过两步反应过程将5-(羟甲基)糠醛(5-HMF)一锅法转化为2,5-双(氨甲基)呋喃(BAF)。发现CuNiAlO是该反应最有效的催化剂,BAF产率为85.9%。我们的结果可以促进生物质资源的可控转化和利用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4cd9/9076022/5258b120a6fb/c9ra08560b-s1.jpg

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