Abstract
An environmentally benign Biginelli reaction for the large-scale preparation of substituted 3,4- dihydropyrimidin-2(1H)-ones using protic acids as a catalyst has been achieved. These mechanochemical reactions proceed efficiently in the absence of organic solvent, with the assistance of infrared lamp irradiation.
Keywords: Biginelli reaction, 3,4-dihydropyrimidin-2-ones, solvent-free reaction, large-scale, mechanochemical reaction, toxicity, dicarbonyl, dihydropyrimidine, aldehyde, carboxylate
Letters in Organic Chemistry
Title: Solvent-Free Biginelli Reaction: A Green Method for the Synthesis of 3,4-Dihydropyrimidin-2-ones Catalyzed by Protic Acids in Large-Scale
Volume: 8 Issue: 4
Author(s): Yangyun Wang, Jipan Yu, Haohao Yang, Zhiwei Miao and Ruyu Chen
Affiliation:
Keywords: Biginelli reaction, 3,4-dihydropyrimidin-2-ones, solvent-free reaction, large-scale, mechanochemical reaction, toxicity, dicarbonyl, dihydropyrimidine, aldehyde, carboxylate
Abstract: An environmentally benign Biginelli reaction for the large-scale preparation of substituted 3,4- dihydropyrimidin-2(1H)-ones using protic acids as a catalyst has been achieved. These mechanochemical reactions proceed efficiently in the absence of organic solvent, with the assistance of infrared lamp irradiation.
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Cite this article as:
Wang Yangyun, Yu Jipan, Yang Haohao, Miao Zhiwei and Chen Ruyu, Solvent-Free Biginelli Reaction: A Green Method for the Synthesis of 3,4-Dihydropyrimidin-2-ones Catalyzed by Protic Acids in Large-Scale, Letters in Organic Chemistry 2011; 8 (4) . https://dx.doi.org/10.2174/157017811795371386
DOI https://dx.doi.org/10.2174/157017811795371386 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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