The Zinin Reduction of Nitroarenes

H. K. Porter
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引用次数: 9

Abstract

The Zinin reduction is a method for the reduction of nitroarenes by negative divalent sulfur. This versatile reaction can be carried out in the laboratory and for plant-scale manufacture of aromatic amines when other reduction media are destructive to sensitive compounds or result in undesired side reactions. The first reaction, used by Zinin, was to prepare aniline from nitrobenzene. It has been of great importance in the preparation of aromatic amines. Refinements in technique and a better understanding of the reaction mechanism should make this method attractive for the preparation of a variety of amines. Keywords: zinin reduction; nitroarenes; side reactions; nitro groups. nitrosoarenes; arylamines; azobenzene reduction; hydrazobenzene; experimental conditions
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硝基芳烃的锌素还原
锌宁还原法是用负二价硫还原硝基芳烃的一种方法。当其他还原介质对敏感化合物具有破坏性或导致不期望的副反应时,这种通用反应可在实验室进行,也可用于芳香胺的工厂规模生产。Zinin使用的第一个反应是从硝基苯中制备苯胺。它在芳香胺的制备中具有重要的意义。技术的改进和对反应机理的更好理解将使该方法对制备各种胺具有吸引力。关键词:锌素还原;nitroarenes;副反应;硝基组。nitrosoarenes;芳基胺;偶氮苯还原;氢化偶氮苯;实验条件
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来源期刊
CiteScore
4.40
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0.00%
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0
期刊最新文献
Cyclization Reactions of Nitrogen‐Centered Radicals Hauser–Kraus, Sammes, Staunton–Weinreb, and Tamura Annulations Enantioselective Hydroformylation Alkene Cross‐Metathesis Reactions The Catalytic Enantioselective Stetter Reaction
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