Sustainable Synthesis of 1,2,3-Triazoles using Cyrene as a Biodegradable Solvent in Click Chemistry.

IF 7.5 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ChemSusChem Pub Date : 2025-01-20 DOI:10.1002/cssc.202402538
Andrea Citarella, Alessandro Fiori, Alessandra Silvani, Daniele Passarella, Valerio Fasano
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引用次数: 0

Abstract

The first successful synthesis of 1,2,3-triazoles using CyreneTM as a biodegradable and non-toxic solvent in click chemistry has been developed. In contrast to previous methods, this sustainable approach allows product isolation by simple precipitation in water, eliminating the need for organic solvent extractions and column chromatography purifications, thus minimizing waste consumption while reducing operational costs. The protocol, performed also at gram scale, has broad applicability and versatility, as shown with complex substrates like biologically active coumarins or triazole-linked bifunctional molecules. Finally, this protocol is also amenable to a three-component reaction involving organic halides, terminal acetylenes and sodium azide, thus avoiding the isolation of organic azides, difficult-to-handle species known for their environmental sensitivity.

以昔苯二烯为生物可降解溶剂可持续合成1,2,3-三唑。
以CyreneTM作为生物可降解的无毒溶剂,首次成功合成了1,2,3-三唑。与以前的方法相比,这种可持续的方法允许通过简单的水中沉淀来分离产品,从而消除了有机溶剂提取和柱层析纯化的需要,从而最大限度地减少了废物消耗,同时降低了运营成本。该方案也在克尺度上进行,具有广泛的适用性和通用性,如生物活性香豆素或三唑连接双功能分子等复杂底物所示。最后,该方案还适用于涉及有机卤化物、末端乙炔和叠氮化物钠的三组分反应,从而避免了有机叠氮化物的分离,这些化合物因其环境敏感性而难以处理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ChemSusChem
ChemSusChem 化学-化学综合
CiteScore
15.80
自引率
4.80%
发文量
555
审稿时长
1.8 months
期刊介绍: ChemSusChem Impact Factor (2016): 7.226 Scope: Interdisciplinary journal Focuses on research at the interface of chemistry and sustainability Features the best research on sustainability and energy Areas Covered: Chemistry Materials Science Chemical Engineering Biotechnology
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