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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288113Generated: October 29, 2026

Thionyl Chloride → 4-(3-Methylbutoxy)benzene-1-sulfonyl chloride

https://huagongshe.com/reaction/2288113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium 4-(3-methylbutoxy)benzenesulfonateHCID 23701366—
CatalystDimethylformamideHCID 6228—
Product4-(3-Methylbutoxy)benzene-1-sulfonyl chlorideHCID 18324001—

Reaction Steps

A mixture of sodium 4-(3-methylbutoxy)benzenesulfonate (2.5 grams, 9.4 mmole), thionyl chloride (10 mL), and 5 drops of N,N-dimethylformamide was heated at reflux for 5 hours. After cooling, the excess thionyl chloride was evaporated and the residue was taken up in ethyl acetate. The solution was cooled in an ice bath and water was added. The organic phase was separated and washed with water and brine. After drying over sodium sulfate, the solvent was evaporated to afford the title compound as an oil, 2.34 grams (95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06087392
Source datasetuspto-grants-2000_07
ORD IDord-7d57581e5cfc4751a6676bd51867cbd1
Source noteuspto-grants-2000_07