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首页> 外文期刊>Combinatorial chemistry & high throughput screening >A green and efficient protocol for the synthesis of quinoxaline, benzoxazole and benzimidazole derivatives using heteropolyanion-based ionic liquids: As a recyclable solid catalyst
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A green and efficient protocol for the synthesis of quinoxaline, benzoxazole and benzimidazole derivatives using heteropolyanion-based ionic liquids: As a recyclable solid catalyst

机译:使用基于杂多阴离子的离子液体合成喹喔啉,苯并恶唑和苯并咪唑衍生物的绿色高效方案:作为可回收的固体催化剂

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摘要

In this paper, we introduce two nonconventional ionic liquid compounds which are composed of propane sulfonate functionalized organic cations and heteropolyanions as green solid acid catalysts for the highly efficient and green synthesis of 2,3-disubstitutedquinoxaline derivatives. These ionic liquids are in the solid state at room temperature and the synthesis is carried out via the one-pot condensation reaction of various o-phenylenediamine with 1,2-diketone derivatives. Benzoxazole and benzimidazole derivatives were also synthesized by these novel catalysts via the one-pot condensation from reaction orthoester with o-aminophenol (synthesis of benzoxazole derivatives) and ophenylenediamine (synthesis of benzimidazole derivatives). All experiments successfully resulted in the desired products. The described novel synthesis method has several advantages of safety, mild condition, high yields, short reaction times, simplicity and easy workup compared to the traditional method of synthesis.
机译:在本文中,我们介绍了两种由丙烷磺酸盐官能化的有机阳离子和杂多阴离子组成的非常规离子液体化合物,作为绿色固体酸催化剂,可高效高效地绿色合成2,3-二取代喹喔啉衍生物。这些离子液体在室温下为固态,并且通过各种邻苯二胺与1,2-二酮衍生物的一锅缩合反应进行合成。这些新催化剂还通过原酸酯与邻氨基苯酚(苯并恶唑衍生物的合成)和邻苯二胺(苯并咪唑衍生物的合成)的一锅缩合反应合成了苯并恶唑和苯并咪唑的衍生物。所有实验均成功产生所需产物。与传统的合成方法相比,所描述的新颖的合成方法具有安全,条件温和,收率高,反应时间短,简单且易于后处理的多个优点。

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