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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675320Generated: October 30, 2026

Nitrobenzene → 3-Nitrobenzenesulfonyl chloride

https://huagongshe.com/reaction/1675320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrobenzeneHCID 7416—
ReactantChlorosulfonic acidHCID 24638—
Product3-Nitrobenzenesulfonyl chlorideHCID 8476—

Reaction Conditions

Temperature82.5 °C

Reaction Steps

Chlorosulfonic acid (4.16 mmol, 0.475 grams) was taken in 1 L three neck round bottom flask equipped with a guard tube and liquid addition funnel. Chlorosulfonic acid was cooled in ice bath to 5-10° C. and nitrobenzene (0.83 mmol, 0.102 grams) was added to the acid slowly, at such a rate that the temperature maintained below 10° C. Reaction mixture was then brought to 25° C. and then slowly heated in an oil bath to 80-85° C. The above reaction mixture was stirred further at 80-85° C. for a period of 3 hours. After completion of the reaction, the reaction mixture was cooled to 10° C. and poured on to the ice-water mixture under stirring, while maintaining the temperature below 10° C. The resulting slurry was then filtered on buchner funnel. The solid cake was dried on phosphorous pentoxide in a desiccator to obtain the title compound as off white solid. Yield: 0.144 grams.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003670B2
Source datasetuspto-grants-2011_08
ORD IDord-af1058c5f35946a8b72d4c3b2c54713d
Source noteuspto-grants-2011_08