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首页> 外文期刊>Environmental chemistry letters >Fast 62-92 % yield preparation of amino acid dithiocarbamates in green solvent at room temperature
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Fast 62-92 % yield preparation of amino acid dithiocarbamates in green solvent at room temperature

机译:在室温下于绿色溶剂中快速制备62-92%的氨基酸二硫代氨基甲酸酯收率

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摘要

Dithiocarbamate and their derivatives are of importance in medicinal chemistry due to their biological activities, in agriculture as fungicides and in organic synthesis as versatile synthetic intermediates. Green solvents such as deep eutectic solvents and polyethylene glycol are new emerging alternatives to conventional harmful organic solvents. Here, we report the synthesis of amino acid-based dithiocarbamates by one-pot three-component reaction of the electrophilic reagent, carbon disulfide and a-amino acids in deep eutectic solvent and polyethylene glycol as a catalyst and reaction media. In situ preparation of dithiocarbamates by the reaction of different amino acids and carbon disulfide, followed by addition reaction with epoxides, alkyl halides and α,β-unsaturated enones at room temperature, gave the corresponding products in 62-92 % yield with a short reaction time without any tedious workup procedures. The deep eutectic solvents and polyethylene glycol were recycled without activity or yield decrease. Therefore, the synthesis of amino acid-based dithiocarbamates in green solvents is a promising alternative to previously used procedures.
机译:由于二硫代氨基甲酸酯及其衍生物的生物活性,它们在药物化学中很重要,在农业中作为杀菌剂,在有机合成中作为通用的合成中间体。绿色溶剂(例如深共熔溶剂和聚乙二醇)是常规有害有机溶剂的新兴替代品。在这里,我们报告了在深共熔溶剂和聚乙二醇作为催化剂和反应介质的情况下,通过亲电试剂,二硫化碳和α-氨基酸的一锅三组分反应合成基于氨基酸的二硫代氨基甲酸酯。通过不同氨基酸与二硫化碳的反应原位制备二硫代氨基甲酸酯,然后在室温下与环氧化物,烷基卤化物和α,β-不饱和烯酮进行加成反应,在短时间内得到相应产物的产率为62-92%时间,无需任何繁琐的检查程序。将深的低共熔溶剂和聚乙二醇再循环而没有活性或产率降低。因此,在绿色溶剂中合成基于氨基酸的二硫代氨基甲酸酯是一种有前途的替代方法。

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