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首页> 外文期刊>RSC Advances >A H2O2/HBr system – several directions but one choice: oxidation–bromination of secondary alcohols into mono- or dibromo ketones
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A H2O2/HBr system – several directions but one choice: oxidation–bromination of secondary alcohols into mono- or dibromo ketones

机译:H2O2 / HBr系统–几个方向但一个选择:氧化-将仲醇溴化为单溴或二溴酮

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In this work we found that a H _(2) O _(2) –HBr(aq) system allows synthesis of α-monobromo ketones and α,α′-dibromo ketones from aliphatic and secondary benzylic alcohols with yields up to 91%. It is possible to selectively direct the process toward the formation of mono- or dibromo ketones by varying the amount of hydrogen peroxide and hydrobromic acid. The convenience of application, simple equipment, multifaceted reactivity, and compliance with green chemistry principles make the application of the H _(2) O _(2) –HBr(aq) system very attractive in laboratories and industry. The proposed oxidation–bromination process is selective in spite of known properties of ketones to be oxidized by the Baeyer–Villiger reaction or peroxidated with the formation of compounds with the O–O moiety in the presence of hydrogen peroxide and Bronsted acids.
机译:在这项工作中,我们发现H _(2)O _(2)–HBr(aq)系统可以从脂肪族和仲苄醇合成α-一溴代酮和α,α'-二溴代酮,收率高达91% 。通过改变过氧化氢和氢溴酸的量,可以有选择地指导该方法趋向于形成一溴或二溴酮。 H _(2)O _(2)–HBr(aq)系统的应用方便,设备简单,反应性多样以及符合绿色化学原理,因此在实验室和工业中非常有吸引力。尽管已知酮的性质会被Baeyer-Villiger反应氧化或在过氧化氢和布朗斯台德酸的存在下与O-O部分形成化合物而被过氧化,但拟议的氧化-溴化工艺是选择性的。

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