氨基酸基离子液体Claisen-Schmidt缩合反应高效合成α, β不饱和酮

Ganesh Gopalsamy Selvaraj, Sakthinarayanan Jayaraman, Uthayanila Selvarasu, Bharathi Priya Velumani, K. Parasuraman
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引用次数: 2

摘要

以可循环L-天冬氨酸偶联咪唑基离子液体为原料,采用Claisen-Schmidt缩合法合成查尔酮是一种绿色合成方法。本研究具有产率高、室温下反应速度加快、催化剂可重复使用、使用无毒试剂等显著优势。查尔酮属黄酮类化合物,具有药理和生物学活性。它包括抗菌、抗真菌、免疫抑制和抗伤害性。离子液体已成为分子有机溶剂的强大工具,液体范围广,易于回收和再利用,使其成为挥发性有机溶剂的更环保的替代品。因此,我们的目标是在本工作中利用它们作为双催化剂和溶剂体系,通过CS缩合合成查尔酮。在一个典型的实验中,苯甲醛(10 mmol)、苯乙酮(10 mmol)和2.5 mol% (L-AAIL)离子液体在50 mL圆底烧瓶中混合。在室温下快速搅拌反应,得到的混合物成为两相体系,残渣在底部,上部含有一些未反应的底物,通过过滤和滗析从催化剂中分离出来。用CH2Cl2萃取催化剂,进行下一个循环的裂解。clisen - schmidt缩合反应在室温下的产率为78% ~ 95%,而传统的缩合反应在1000℃以上时进行,[L-AAIL]是一种高效、环保的室温合成查尔酮衍生物催化剂。[L-AAIL]作为溶剂和催化剂将展示出真正的优势,它提供了一个“绿色”的过程,操作更安全,反应周期短,反应条件温和,更容易分离,离子液体的可重复使用,使该方法对合成有机化学家和工业有价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Efficient Synthesis Of α, β Unsaturated Ketones Via Claisen–Schmidt Condensation Reaction Using Amino Acid Based Ionic Liquids
Synthesis of chalcone by Claisen–Schmidt condensation using recyclable L- aspartic acid coupled imidazolium-based ionic liquid as a green synthetic approach has been developed. Present work offers significant advantages such as high yield, enhanced reaction speed even at room temperature, catalyst reusability, and the involvement of non-toxic reagents. Chalcones are a flavonoid family and have pharmacological and biological activities. It includes antibacterial, antifungal, immunosuppressive, and anti-nociceptive properties. Ionic liquid has emerged as a powerful tool for molecular organic solvents and wide liquid range, ease of recovery and reuse, and making them a greener alternative to volatile organic solvents. Thus, our objective was to employ them as dual catalyst and solvent systems to synthesize chalcone via CS condensation in the present work. In a typical experiment, benzaldehyde (10 mmol), acetophenone (10 mmol), and 2.5 mol% (L-AAIL) ionic liquid were mixed in a 50 mL round-bottom flask. The reaction was preceded quickly at room temperature with stirring, the resulting mixture became a biphasic system with the residue at the bottom and the upper phase containing some unreacted substrate separated from the catalyst by filtration and decantation. The catalyst was extracted with CH2Cl2 and split for the next cycle. Claisen–Schmidt condensation accomplished with reasonable to good yields, ranged from 78 to 95% at room temperature in the presence of the [L-AAIL], as compared to the traditional route at more than 100O C. [L-AAIL] are found a highly efficient and eco-friendly catalyst for synthesizing chalcone derivatives at room temperature. [L-AAIL] as a solvent and catalyst will exhibit real advantages by providing a ‘green’ process with the safer operation, Short reaction periods, mild reaction conditions, easier separation, and reusability of ionic liquid made this methodology valuable for synthetic organic chemists as well as industry.
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