REACTION OF 1-ARYL-2-ALKENYLDIAZENE 1-OXIDES WITH HYDROGEN-CHLORIDE - NOVEL-APPROACH TO THE SYNTHESIS OF FUNCTIONALLY-SUBSTITUTED ARYLHYDRAZONES

被引：1

作者：

TYURIN, AY ^{[1
]}

CHURAKOV, AM ^{[1
]}

GONCHAROVA, EL ^{[1
]}

IOFFE, SL ^{[1
]}

STRELENKO, YA ^{[1
]}

机构：

[1] RUSSIAN ACAD SCI,ND ZELINSKII ORGAN CHEM INST,MOSCOW 117913,RUSSIA

来源：

RUSSIAN CHEMICAL BULLETIN | 1995年 / 44卷 / 05期

关键词：

CHLOROHYDRAZONES; DIAZENE OXIDES; AZOXYALKANES; AZOOLEFINS;

D O I：

10.1007/BF00696924

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The reaction of 1-aryl-2-alkenyldiazene 1-oxides with HCl yields arylhydrazones of alpha-chloroacyl chlorides, which eliminate HCl to give 1-aryl-2-(1-chloroalken-1-yl)diazenes. The latter add amines, alcohols, and carboxylic acids to give arylhydrazone chlorides with alpha-functional groups.

引用

页码：901 / 906

页数：6

共 6 条

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