The action of sulphur monochloride on o-nitroanilines and o-phenylenediamines: the formation of 2,1,3-benzothiadiazoles

P. Hope
, 
L A Wiles
Тип публикации: Journal Article
Дата публикации: 1966-01-01
Royal Society of Chemistry (RSC)
SJR: —
CiteScore: —
Impact factor: —
ISSN: 00224952
Organic Chemistry
Краткое описание
o-Phenylenediamines react with sulphur monochloride forming 2,1,3-benzothiadiazoles. In acid solution the nitro-group of o-nitroanilines oxidises sulphur monochloride to thionyl chloride, and the phenylenediamine thus formed reacts with these sulphur compounds giving the corresponding benzothiadiazole.
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Hope P., Wiles L. A. The action of sulphur monochloride on o-nitroanilines and o-phenylenediamines: the formation of 2,1,3-benzothiadiazoles // Journal of the Chemical Society C Organic. 1966. p. 1283.
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Hope P., Wiles L. A. The action of sulphur monochloride on o-nitroanilines and o-phenylenediamines: the formation of 2,1,3-benzothiadiazoles // Journal of the Chemical Society C Organic. 1966. p. 1283.
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TY - JOUR
DO - 10.1039/j39660001283
UR - https://doi.org/10.1039/j39660001283
TI - The action of sulphur monochloride on o-nitroanilines and o-phenylenediamines: the formation of 2,1,3-benzothiadiazoles
T2 - Journal of the Chemical Society C Organic
AU - Hope, P.
AU - Wiles, L A
PY - 1966
DA - 1966/01/01
PB - Royal Society of Chemistry (RSC)
SP - 1283
SN - 0022-4952
ER -
BibTex
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@article{1966_Hope,
author = {P. Hope and L A Wiles},
title = {The action of sulphur monochloride on o-nitroanilines and o-phenylenediamines: the formation of 2,1,3-benzothiadiazoles},
journal = {Journal of the Chemical Society C Organic},
year = {1966},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/j39660001283},
pages = {1283},
doi = {10.1039/j39660001283}
}