The synthesis and reactions of some polychloroaromatic azides, sulphonyl azides and sulphonohydrazides

Author:

Bernard IRA,Chivers GE,Cremlyn RJW,Mootoosamy KG

Abstract

Azidopentachlorobenzene (2) and 4-azidotetrachloropyridine (4) react with norbornene to give the aziridines (6) and (7); with cyclohexene the enamines (10) and (11) are formed. 1,2,3,4-Tetrachlorobenzene reacts with chlorosulphonic acid to give 2,3,4,5-tetrachlorobenzenesulphonyl chloride (14), but the reported chlorosulphonation of 1,2,4,5-tetrachlorobenzene could not be effected, and under drastic conditions the reaction afforded hexachlorobenzene. The sulphonyl chloride (14) reacts with hydrazine to give the sulphonohydrazide (15). However, in contrast to previous work, reaction of polychloroaromatic sulphonyl chlorides with ammonia and phenylhydrazine gave only the normal sulphonamides and N'-phenyl sulphonohydrazides.

Publisher

CSIRO Publishing

Subject

General Chemistry

Cited by 16 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Utility of pentachloropyridine in organic synthesis;Journal of the Iranian Chemical Society;2020-03-27

2. A Convenient Synthesis of High-Purity 1-Chloro-2,6-difluorobenzene;Organic Process Research & Development;2003-09-06

3. Mono-, Di-, and Trinitrenes in the Pyridine Series;Journal of the American Chemical Society;2000-02-08

4. Synthesis and regioselective cycloaddition reactions of 2,4,6-triazido-3,5-dichloropyridine;Mendeleev Communications;1999-01

5. Stereo- and regioselective cycloaddition of norbornene to 2,4,9-triazidopyridine;Chemistry of Heterocyclic Compounds;1997-11

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