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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662731Generated: October 30, 2026

Chlorosulfonic acid → HCID 86625712, compound

https://huagongshe.com/reaction/1662731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantHCID 67428671HCID 67428671—
SolventChloroformHCID 6212—
ProductHCID 86625712HCID 86625712—
ProductHCID 86625713HCID 86625713—

Reaction Steps

To a solution of 1.00 g of the compound obtained in Step 179-1 in CHCl3 (10 ml) was added dropwise 3.36 g of chlorosulfonic acid in CHCl3 (10 ml) over 30 minutes under ice cooling. After stirring at room temperature for one hour, the solution was poured into ice water and the resulting mixture was extracted with CHCl3. The organic layer was washed with a saturated aqueous solution of NaHCO3 and with saturated brine and then dried over MgSO4; the drying agent was separated by filtration, and then the solvent was evaporated under reduced pressure. The obtained residue was purified by column chromatography (silicagel 60N; mobile phase: EtOAc/n-hexane=1/10 to 1/5; v/v) to obtain 340 mg of 4-(methylthio)-2-(trifluoromethoxy)benzene sulfonyl chloride (179-2-a) and 212 mg of 2-(methylthio)-4-(trifluoromethoxy)benzene sulfonyl chloride (179-2-b).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030499B2
Source datasetuspto-grants-2011_10
ORD IDord-cae0664ff36c4cb4a839c2ec3e233759
Source noteuspto-grants-2011_10