抗坏血酸钠辅助下苯磺酰叠氮化物转化为磺酰胺的电化学研究

IF 0.4 4区 化学 Q4 CHEMISTRY, ORGANIC
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引用次数: 0

摘要

化学还原有机叠氮化物是合成有机化学中制备氨基化合物的常用途径。研究人员和科学家对在有机分子合成过程中选择更绿色的途径感兴趣。本文报道了用铂电极电化学还原叠氮化苯磺酰基合成苯磺酰胺。研究了电流密度和电压、电解质、溶剂和底物浓度对产物收率的影响。当抗坏血酸钠存在时(甲醇-水比例为1:1),该反应更可行,在电化学过程中,抗坏血酸钠既是支撑电解质,又是电子转移剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrochemical conversion of benzene sulphonyl azide into sulphonamide assisted by sodium ascorbate
Chemical reduction of organic azides is a commonly accepted route in synthetic organic chemistry to prepare amino compounds. Researchers and scientists are interested in choosing greener pathways in the course of the synthesis of organic molecules. In the present work we report the synthesis of benzene sulphonamide by the electrochemical reduction of benzene sulphonyl azide using platinum electrodes. Influence of current density and voltage, effect of electrolytes, effect of solvents and effect of substrate concentration on the yield of the product have been studied. The reaction is more feasible in the presence of sodium ascorbate (in 1:1 methanol-water) which acts as both supporting electrolyte and electron transferring agent in the electrochemical process.
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