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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8633Generated: October 23, 2026

Dichloromethane → 2,5-Dichloro-4-methylthiophene-3-sulfonyl chloride

https://huagongshe.com/en/reaction/8633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant3-MethylthiopheneHCID 12024—
ReactantChlorosulfonic acidHCID 24638—
ReactantSulfuryl chlorideHCID 24648—
Product2,5-Dichloro-4-methylthiophene-3-sulfonyl chlorideHCID 2198379625%

Reaction Conditions

Temperature10 °C

Reaction Steps

To a cooled (10° C.) solution of 3-methylthiophene (5 g, 50 mmol) in dichloromethane (15 mL) was added a solution of sulfuryl chloride (8.6 mL) in dichloromethane (5 mL). The reaction mixture was maintained at 10° C. for 30 minutes, then at ambient temperature for 16 hours. The reaction was concentrated and redissolved in dichloromethane (30 mL) and cooled to −10° C. To the cooled solution was added chlorosulfonic acid (2 mL, 100 mmol). The reaction was maintained at −10° C. for 30 minutes, then at ambient temperature for 16 hours, at which time it was poured into ice water (50 mL) and extracted with dichloromethane (50 mL). The organic layer was dried (Mg2SO4) and concentrated to furnish a brown oil (3.3 g, 25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091204B2
Source datasetuspto-grants-2006_08
ORD IDord-d3a94c6cd2a949a99cb74eb9ff971a3b
Source noteuspto-grants-2006_08