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在点击化学中使用环丁砜作为可生物降解溶剂可持续合成1,2,3-三唑。

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

作者信息

Citarella Andrea, Fiori Alessandro, Silvani Alessandra, Passarella Daniele, Fasano Valerio

机构信息

Dipartimento di Chimica, Università degli Studi di Milano, Via Golgi 19, 20133, Milano, Italy.

出版信息

ChemSusChem. 2025 May 19;18(10):e202402538. doi: 10.1002/cssc.202402538. Epub 2025 Jan 31.

Abstract

The first successful synthesis of 1,2,3-triazoles using Cyrene 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.

摘要

已开发出在点击化学中使用环丁砜作为可生物降解且无毒的溶剂首次成功合成1,2,3 - 三唑的方法。与以前的方法相比,这种可持续的方法允许通过在水中简单沉淀来分离产物,无需有机溶剂萃取和柱色谱纯化,从而在降低运营成本的同时最大限度地减少废物消耗。该方案也能以克级规模进行,具有广泛的适用性和多功能性,如具有生物活性的香豆素或三唑连接的双功能分子等复杂底物所示。最后,该方案也适用于涉及有机卤化物、末端炔烃和叠氮化钠的三组分反应,从而避免了有机叠氮化物的分离,有机叠氮化物是已知对环境敏感且难以处理的物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd3b/12094146/3f4b869e054a/CSSC-18-e202402538-g003.jpg

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