在无溶剂条件下,以l -阿拉伯糖为可再生催化剂,通过Biginelli反应绿色可持续合成3,4-二氢嘧啶-2(1H)-酮/硫酮

IF 1.8 3区 化学 Q3 CHEMISTRY, ORGANIC
Priya C. Saroj , Sai Srinivas Ponugoti , Shivangi Sawant , Shreerang V. Joshi
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引用次数: 0

摘要

在追求可持续的有机合成方法的过程中,可再生和可生物降解催化剂的应用受到了极大的关注。本文报道了在无溶剂环境下,以环境友好型催化剂l -阿拉伯糖为原料,通过Biginelli反应合成3,4-二氢嘧啶-2(1H)-酮/硫酮。l -阿拉伯糖是一种天然存在的糖,它能有效地催化β-酮酯和醛与尿素或硫脲的缩合反应,生成产率高、原子经济性好的二聚庚烷。反应在温和的温度下进行得很有效,催化剂很容易再生,可以进行多次催化循环。l -阿拉伯糖的使用不仅避免了有毒溶剂和金属催化剂,而且由于可再生资源的开发,实现了绿色化学。这是可持续催化领域向前迈出的重要一步,并为合成dhpm提供了一种环境友好且操作简单的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Green and sustainable synthesis of 3,4-Dihydropyrimidin-2(1H)-ones/thiones via the Biginelli reaction using L-arabinose as a renewable catalyst under solvent-free conditions
In the pursuit of sustainable methodologies in organic synthesis, the application of renewable and biodegradable catalysts has received significant attention. This work processes the synthesizing of 3,4-dihydropyrimidin-2(1H)-ones/thiones using L-arabinose, an environment-friendly catalyst via the Biginelli reaction in a solvent-free environment is reported herein. L-arabinose, a naturally occurring sugar, efficiently catalyzes the condensation reaction between β-ketoesters and aldehyde with urea or thiourea to form DHPMs with high yields and excellent atom economy. The reaction proceeds efficiently at mild temperatures, and the catalyst is easily regenerated, enabling multiple catalytic cycles. The use of L-arabinose avoids not only toxic solvents and metal catalysts but also processes green chemistry due to the exploitation of renewable resources. It is a significant step forward in the domain of sustainable catalysis and provides an environmentally benign and operationally simple procedure for the synthesis of DHPMs.
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来源期刊
Synthetic Communications
Synthetic Communications 化学-有机化学
CiteScore
4.40
自引率
4.80%
发文量
156
审稿时长
4.3 months
期刊介绍: Synthetic Communications presents communications describing new methods, reagents, and other synthetic work pertaining to organic chemistry with sufficient experimental detail to permit reported reactions to be repeated by a chemist reasonably skilled in the art. In addition, the Journal features short, focused review articles discussing topics within its remit of synthetic organic chemistry.
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