Green electrosynthesis of bis(indolyl)methane derivatives in deep eutectic solvents

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY BMC Chemistry Pub Date : 2024-07-27 DOI:10.1186/s13065-024-01245-9
Mina E. Adly, Amr M. Mahmoud, Hala B. El-Nassan
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Abstract

In this study, a new green method was developed for the synthesis of bis(indolyl)methane derivatives using electrochemical bisarylation reaction in deep eutectic solvents as a green alternative to traditional solvents and electrolytes. The effects of varying time, current, type of solvent and material of electrodes were all studied. The optimum reaction conditions involved the use of ethylene glycol/choline chloride with a ratio of 2:1 at 80 °C for 45 min. Graphite and platinum were used as cathode and anode, respectively. The newly developed method offered many advantages such as using mild reaction conditions, short reaction time and affording high product yields with a wide range of substituted aromatic aldehydes bearing electron donating or electron withdrawing substituents. In addition, the electrochemical method proved to be more effective than heating in deep eutectic solvents and afforded higher yields of products in shorter reaction time. The mechanism of the electrochemical reaction was proposed and confirmed using the cyclic voltammetry study.

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在深共晶溶剂中绿色电合成双(吲哚基)甲烷衍生物
本研究开发了一种在深共晶溶剂中利用电化学双芳基化反应合成双(吲哚基)甲烷衍生物的新型绿色方法,作为传统溶剂和电解质的绿色替代品。研究了不同时间、电流、溶剂类型和电极材料的影响。最佳反应条件是使用乙二醇/氯化胆碱比例为 2:1,在 80 °C 下反应 45 分钟。石墨和铂分别用作阴极和阳极。新开发的方法具有许多优点,如反应条件温和、反应时间短、产品收率高,可处理多种带有供电子或退电子取代基的取代芳醛。此外,事实证明电化学方法比在深共晶溶剂中加热更有效,而且反应时间更短,产物收率更高。通过循环伏安法研究,提出并证实了电化学反应的机理。
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来源期刊
BMC Chemistry
BMC Chemistry Chemistry-General Chemistry
CiteScore
5.30
自引率
2.20%
发文量
92
审稿时长
27 weeks
期刊介绍: BMC Chemistry, formerly known as Chemistry Central Journal, is now part of the BMC series journals family. Chemistry Central Journal has served the chemistry community as a trusted open access resource for more than 10 years – and we are delighted to announce the next step on its journey. In January 2019 the journal has been renamed BMC Chemistry and now strengthens the BMC series footprint in the physical sciences by publishing quality articles and by pushing the boundaries of open chemistry.
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