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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163203Generated: October 30, 2026

2-Nitroanisole → Benzenesulfonyl chloride, 4-methoxy-3-nitro-

https://huagongshe.com/reaction/2163203

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitroanisoleHCID 7048—
ReactantChlorosulfonic acidHCID 24638—
ProductBenzenesulfonyl chloride, 4-methoxy-3-nitro-HCID 89600—

Reaction Conditions

Temperature0 °C

Reaction Steps

2.5 mols (165 ml ) of chlorosulphonic acid are placed in a one-liter reaction vessel equipped with a stirring system, a thermometer and a dropping funnel and the acid is cooled to about 0° C with a mixture of ice and salt. 0.8 mol (100 ml) of 2-nitroanisole is added drop by drop and the solution is then allowed to come back to room temperature; after a contact time of 30 minutes, the reaction mixture is poured onto one fifth of its volume of crushed ice. The sulphonyl chloride precipitates in the form of an oil; this is extracted with chloroform. After evaporation of the organic phase, the sulphonyl chloride is crystallized in a benzene/petroleum ether mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04132786
Source datasetuspto-grants-1979_01
ORD IDord-804bbe9da8604ec194c3a8a52d4891dd
Source noteuspto-grants-1979_01