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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408367Generated: October 29, 2026

Chlorosulfonic acid → 1187082-98-9

https://huagongshe.com/reaction/2408367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantBenzene, 1-fluoro-2-methyl-4-nitro-HCID 68001—
Product1187082-98-9HCID 57562880—

Reaction Conditions

Temperature110 °C

Reaction Steps

A dry reaction flask equipped with a stirring bar, a reflux condenser and nitrogen inlet was charged with 4-fluoro-3-methylnitrobenzene (25) (3.10 g, 20 mmol). To this at 0° C., was added dropwise chlorosulfonic acid (5.29 mL, 80 mmol) over a period of 15 minutes. After bringing the homogeneous solution to room temperature, it was stirred at 110° C. for 24 hours. The resulting slurry was then poured over ice water (100 gm), extracted with diethyl ether (3×75 mL), and the organic phase washed with water (75 mL), then dried over anhydrous sodium sulfate. The solvent was then removed under reduced pressure to afford the corresponding sulfonyl chloride derivative (26), which was used further without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815848B2
Source datasetuspto-grants-2014_08
ORD IDord-e9680b51203e4d74aa89d5fafd988602
Source noteuspto-grants-2014_08