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首页> 外文期刊>RSC Advances >Electroselective α-bromination of acetophenone using in situ bromonium ions from ammonium bromide
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Electroselective α-bromination of acetophenone using in situ bromonium ions from ammonium bromide

机译:溴化铵的原位溴离子的电溶α-溴化α-溴化

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A greener and expeditious method for the side chain bromination of acetophenone using in situ generated bromonium ions from NH _(4) Br and a catalytic amount of H _(2) SO _(4) as a supporting electrolyte in a H _(2) O:CH _(3) CN medium at ambient temperature has been developed in an undivided cell equipped with a Pt/Pt electrode. This method results in a good yield (80%) of α-bromo acetophenone with high selectivity when only 2 F of electricity was passed. Optimization studies such as variation of the current density, charge passed, solvent, solvent/water ratio, acid, acid strength, bromide salt, bromide salt concentration, etc. , are carried out and reported.
机译:一种绿色且迅速的方法,用于苯乙酮的侧链溴化溴代,原位产生的溴离子与来自NH _(4)Br的催化量H _(2)SO _(4)作为H_(2)的支撑电解质(2 )O:CH _(3)在环境温度下的CN培养基已经在配备有Pt / Pt电极的未分割的细胞中开发。该方法产生良好的产率(80%)α-溴乙酮,当仅通过2f时具有高选择性。优化研究,如电流密度,电荷,溶剂,溶剂,溶剂/水比,酸,酸强度,溴化物,溴化物浓度等的变化和报道。

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