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无溶剂条件下碳基固体酸催化一锅法合成酰胺烷基萘酚(英文)
作者姓名:Abolghasem Davoodnia  Rahil Mahjoobin  Niloofar Tavakoli-Hoseini
作者单位:Department of Chemistry, Faculty of Sciences, Mashhad Branch, Islamic Azad University, Mashhad, Iran
基金项目:supported by Islamic Azad University, Mashhad Branch
摘    要:An efficient, environmentally friendly procedure for the synthesis of amidoalkyl naphthols through the one‐pot, three‐component reaction of β‐naphthol, aryl aldehydes, and acetamide in the presence of a carbon‐based solid acid under thermal solvent‐free conditions is described. The beneficial fea-tures of this new synthetic approach include short reaction time, high yields, clean reaction profiles, and a simple work‐up procedure. Furthermore, the catalyst can be readily recycled and reused four times without obvious significant loss of activity. The structure of the catalyst was confirmed by Fourier transform infrared spectroscopy, N2 adsorption/desorption analysis, and X‐ray diffraction.

关 键 词:Amidoalkyl  naphthol  Carbon‐based  solid  acid  Heterogeneous  catalysis  Solvent‐free  condition
收稿时间:2013-10-18

A facile,green, one-pot synthesis of amidoalkyl naphthols under solvent-free conditions catalyzed by a carbon-based solid acid
Abolghasem Davoodnia,Rahil Mahjoobin,Niloofar Tavakoli-Hoseini.A facile,green, one-pot synthesis of amidoalkyl naphthols under solvent-free conditions catalyzed by a carbon-based solid acid[J].Chinese Journal of Catalysis,2014,35(4):490-495.
Authors:Abolghasem Davoodnia  Rahil Mahjoobin  Niloofar Tavakoli-Hoseini
Institution:Department of Chemistry, Faculty of Sciences, Mashhad Branch, Islamic Azad University, Mashhad, Iran
Abstract:An efficient, environmentally friendly procedure for the synthesis of amidoalkyl naphthols through the one-pot, three-component reaction of β-naphthol, aryl aldehydes, and acetamide in the presence of a carbon-based solid acid under thermal solvent-free conditions is described. The beneficial features of this new synthetic approach include short reaction time, high yields, clean reaction profiles, and a simple work-up procedure. Furthermore, the catalyst can be readily recycled and reused four times without obvious significant loss of activity. The structure of the catalyst was confirmed by Fourier transform infrared spectroscopy, N2 adsorption/desorption analysis, and X-ray diffraction.
Keywords:Amidoalkyl naphthol  Carbon-based solid acid  Heterogeneous catalysis  Solvent-free condition
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