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Kinetic and mechanistic study of bromination of sulfanilic acid with N-bromosuccinimide in alkaline medium

机译:N-溴代琥珀酰亚胺在碱性介质中溴化磺胺酸的动力学和机理研究

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摘要

The sulfanilic acid (p-amino benzene sulfonic acid) (SNA) is an important and interesting compound which finds a number of applications in the syntheses of organic dyes. The amide of sulfanilic acid (sulfanilamide) and certain related substituted amides are of considerable medicinal importance as the sulfa drugs. The kinetics of bromination of SNA with N-bromosuccinimide (NBS) in NaOH medium has been studied at 308 K. The experimental rate law obtained is -dNBS]/dt =NBS]SNA](x)OH(-)] where x is less than unity. The reaction was subjected to changes in concentration of succinimide, the reduction product of NBS, concentration of added neutral salt, as well as to dielectric permittivity and ionic strength of the medium. Solvent isotope effect has been studied using D(2)O. The stoichiometry of the reaction has been determined, and the products were identified and characterized. Activation parameters for the overall reactions have been computed using the Arrhenius plot. OBr(-) has been postulated as the reactive species of NBS. The reaction fails to induce polymerization of added acrylonitrile. The proposed mechanism and the derived rate law are consistent with the observed kinetic data.
机译:磺胺酸(对氨基苯磺酸)(SNA)是一种重要而有趣的化合物,在有机染料的合成中有许多应用。磺胺酸的酰胺(磺胺)和某些相关的取代酰胺作为磺胺类药物具有重要的医学意义。已在308 K下研究了N-溴代琥珀酰亚胺(NBS)在NaOH介质中溴化SNA的动力学。获得的实验速率定律为-dNBS] / dt = NBS] SNA](x)OH(-)],其中x为不到团结。使反应经受琥珀酰亚胺浓度,NBS还原产物,添加的中性盐浓度以及介质的介电常数和离子强度的变化。已使用D(2)O研究了溶剂的同位素效应。已确定反应的化学计量,并鉴定和表征了产物。总体反应的激活参数已使用Arrhenius图进行了计算。 OBr(-)被假定为NBS的反应性物质。该反应不能引起添加的丙烯腈的聚合。所提出的机理和导出的速率定律与观察到的动力学数据一致。

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