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基于原儿茶酸的低共熔溶剂介导的1,2,4,5-四取代咪唑的绿色合成

The protocatechuic acid-based deep eutectic solvent-mediated green synthesis of 1,2,4,5-tetrasubstituted imidazoles.

作者信息

Goudarzi Hadis, Habibi Davood, Monem Arezo

机构信息

Department of Organic Chemistry, Faculty of Chemistry and Petroleum Sciences, Bu-Ali Sina University Hamedan 6517838683 Iran

出版信息

RSC Adv. 2024 Jul 16;14(31):22459-22469. doi: 10.1039/d4ra03302g. eCollection 2024 Jul 12.

Abstract

A novel protocatechuic acid-based deep eutectic solvent (ETPPBr/PCA-DES) was prepared by mixing ethyltriphenylphosphonium bromide (ETPPBr) and protocatechuic acid (PCA = 3,4-dihydroxybenzoic acid), and its structure was fully investigated by using the FT-IR, TGA/DTA, densitometer, eutectic point and H NMR techniques. Different molar ratios of ETPPBr to PCA were examined and the eutectic point phase diagram showed that the best ratio for the synthesis of the new DES is the one-to-one ratio of the two starting materials (ETPPBr and PCA). Then, the novel DES was used as a new and capable catalyst for the green synthesis of diverse 1,2,4,5-tetrasubstituted imidazoles a1-a12 from the four-component condensation reaction of phenanthrene-9,10-dione, aromatic amine, aromatic aldehyde, and ammonium acetate with high yields and very short reaction times. High yields and very short reaction times are two advantages of our proposed method compared with the previous reported methods.

摘要

通过将乙基三苯基溴化鏻(ETPPBr)和原儿茶酸(PCA = 3,4-二羟基苯甲酸)混合制备了一种新型的基于原儿茶酸的低共熔溶剂(ETPPBr/PCA-DES),并使用傅里叶变换红外光谱(FT-IR)、热重/差示热分析(TGA/DTA)、密度计、低共熔点和核磁共振氢谱(H NMR)技术对其结构进行了全面研究。考察了ETPPBr与PCA的不同摩尔比,低共熔点相图表明,合成新型低共熔溶剂的最佳比例是两种原料(ETPPBr和PCA)的一对一比例。然后,将这种新型低共熔溶剂用作一种新型且高效的催化剂,用于从菲-9,10-二酮、芳香胺、芳香醛和乙酸铵的四组分缩合反应中绿色合成多种1,2,4,5-四取代咪唑a1-a12,产率高且反应时间非常短。与先前报道的方法相比,高收率和极短的反应时间是我们所提出方法的两个优点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2418/11249645/42cfc8a06950/d4ra03302g-s1.jpg

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