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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703736Generated: October 31, 2026

1-Chloro-2-nitrobenzene → Benzenesulfonyl chloride, 4-chloro-3-nitro-

https://huagongshe.com/reaction/1703736

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-2-nitrobenzeneHCID 6945—
ReactantChlorosulfonic acidHCID 24638—
ProductBenzenesulfonyl chloride, 4-chloro-3-nitro-HCID 7323—

Reaction Steps

On the other hand, those compounds of formula (1) wherein X is hydroxy and A is a sulfonamido group can be prepared by treating, for example, ortho-nitro-chlorobenzene with chlorosulfonic acid to obtain 3-nitro-4-chlorobenzenesulfonylchloride, followed by treatment with a primary or secondary amine to yield the corresponding 3-nitro-4-chlorobenzene sulfonamido derivative. This product is then treated with caustic soda to yield the 3-nitro-4-hydroxybenzene sulfonamide and subsequently reduced to the desired 3-amino-4-hydroxybenzene sulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04125368
Source datasetuspto-grants-1978_11
ORD IDord-efbcd231dfc544c690ced9941717a8a9
Source noteuspto-grants-1978_11