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首页> 外文期刊>Catalysis Letters >Amino Acid Amide based Ionic Liquid as an Efficient Organo-Catalyst for Solvent-free Knoevenagel Condensation at Room Temperature
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Amino Acid Amide based Ionic Liquid as an Efficient Organo-Catalyst for Solvent-free Knoevenagel Condensation at Room Temperature

机译:氨基酸酰胺基离子液体作为高效有机催化剂,用于室温下的无溶剂knoevenage凝聚

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摘要

Ionic liquids of amino acid amide were synthesized and used as an efficient catalyst for solvent-free Knoevenagel condensation. Synthesized ionic liquids are an environmentally benign, inexpensive, metal free and plays the dual role of solvent as well as an efficient catalyst for Knoevenagel condensation. A wide range of aliphatic, aromatic and heteroaromatic aldehydes easily undergo condensation with malononitrile and ethyl cyanoacetate. The reaction proceeds at room temperature without using any organic solvent and is very fast with good to excellent yield. Additionally, the catalyst is easily separable and recyclable without loss of activity.
机译:合成氨基酸酰胺的离子液体,用作无溶剂knoevenagel缩合的有效催化剂。 合成的离子液体是环境良好,廉价的,无含金属,并发挥溶剂的双重作用以及knoevenagel冷凝的有效催化剂。 各种脂族,芳族和杂芳醛容易用丙二腈和氰基乙酸乙酯进行缩合。 反应在室温下进行而不使用任何有机溶剂,并且非常快,良好至优异的产率。 另外,催化剂容易分离和可回收而不会丧失活性。

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