Kinetics and mechanism of deoximation of benzophenone oximes by N-chloro-3-methyl-2,6-diphenylpiperidin-4-one

被引：0

作者：

Kabilan, S ^{[1
]}

Vasanthi, G ^{[1
]}

Suganya, K ^{[1
]}

Palanivel, C ^{[1
]}

机构：

[1] Annamalai Univ, Dept Chem, Annamalainagar 608002, Tamil Nadu, India

来源：

OXIDATION COMMUNICATIONS | 2000年 / 23卷 / 04期

关键词：

deoximation; benzophenone oximes; N-chloro-3-methyl-2,6-diphenylpiperidin-4-one; mechanism; correlation analysis;

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Deoximation of benzophenone oxime (BPO) and several of its para-substituted derivatives by N-chloro-3-methyl-2,6-diphenylpiperidin-4-one (NCP) yields respective ketones. The stoichiometry of the reaction was found to be 1:1 and the order with respect to [substrate] and [oxidant] was found to be one each. Increasing [H+] and [Cl-] increases the rate of the reaction. Increasing the percentage of ethanol decreases the rate of the reaction. The mechanistic pathways of the reaction have been discussed and substantiated through multiparameter correlation analysis of the substituted effect.

引用

页码：524 / 531

页数：8

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