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Benzoin condensation in 1,3-dialkylimidazolium ionic liquids via electrochemical generation of N-heterocyclic carbene

机译:通过N-杂环卡宾的电化学反应生成1,3-二烷基咪唑鎓离子液体中的苯偶姻缩合

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摘要

N-heterocyclic carbenes generated by electrochemical reduction under galvanostatic control of 1,3-dial kylimidazolium-based ionic liquids were employed as organocatalysts in the benzoin condensation reac tion. Benzoin was isolated in a good yield (84%) by a catalytic amount of carbene (20%). The use of toxic, volatile molecular solvents as well as any addition of bases has been avoided.
机译:在苯偶姻缩合反应中,通过在恒电流控制下1,3-二甲苯基咪唑鎓离子液体的电化学还原作用下电化学还原生成的N-杂环卡宾用作有机催化剂。通过催化量的卡宾(20%)以良好的收率(84%)分离出苯偶姻。避免使用有毒,易挥发的分子溶剂以及任何碱的添加。

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