Advancements in Green Chemistry: Microwave-Assisted Synthesis of Poly-Heterocyclic Compounds in Aqueous Media

Mohamed R. Eletmany
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Abstract

This comprehensive review explores the recent strides made in the field of green chemistry, focusing on the utilization of microwave (MW) irradiation for the synthesis of poly-heterocyclic compounds in aqueous media. The adoption of environmentally benign protocols involving greener alternatives has led to significant reductions in chemical waste and reaction time. The review highlights various methodologies, such as the MW-assisted synthesis of nitrogen-containing heterocycles, cyclic ureas, triazoles, dihydropyrimidinones, oxygen heterocycles, tetrahydropyrans, and heterocyclic hydrazones. The synthesis of diverse heterocyclic structures is accomplished through innovative strategies, including N-alkylation, direct Grignard-type addition, and three-component condensation reactions. The review emphasizes the advantages of these approaches, such as shorter reaction times, higher product yields, and the elimination of hazardous organic solvents. Additionally, the use of recyclable catalysts, such as montmorillonite K10 clay and nano-sized magnesium oxide, contributes to the eco-friendly nature of the methodologies. The incorporation of green synthesis principles, including water-mediated conditions and catalyst recyclability, reflects a commitment to sustainable and efficient synthetic practices. This review provides valuable insights into the ongoing efforts to minimize the environmental footprint of chemical synthesis while advancing the field of heterocyclic compound synthesis.
绿色化学的进展:在水介质中微波辅助合成多杂环化合物
本综述探讨了绿色化学领域最近取得的进展,重点是利用微波(MW)辐照在水介质中合成多杂环化合物。采用绿色替代品的环境友好方案大大减少了化学废物和反应时间。本综述重点介绍了各种方法,如分子水溶液辅助合成含氮杂环、环脲、三唑、二氢嘧啶酮、含氧杂环、四氢呋喃和杂环肼。各种杂环结构的合成是通过创新策略完成的,包括 N-烷基化、直接格氏加成和三组分缩合反应。综述强调了这些方法的优势,如反应时间更短、产品产率更高、无需使用有害有机溶剂。此外,使用可回收催化剂(如蒙脱石 K10 粘土和纳米级氧化镁)也有助于实现这些方法的生态友好性。绿色合成原则,包括水介导条件和催化剂可回收性,体现了对可持续和高效合成实践的承诺。这篇综述为我们在推进杂环化合物合成领域的同时,最大限度地减少化学合成对环境的影响提供了宝贵的见解。
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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