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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251673Generated: October 27, 2026

Chlorosulfonic acid → 3-methoxythiophene-2-sulfonyl Chloride

https://huagongshe.com/reaction/1251673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPhosphorus pentachlorideHCID 24819—
Reactant3-MethoxythiopheneHCID 140249—
SolventChloroformHCID 6212—
Product3-methoxythiophene-2-sulfonyl ChlorideHCID 1129882243.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Chlorosulfonic acid (ClSO3H, 2.31 g, 19.62 mmol) was slowly added to a solution of 3-methoxythiophene (2.29 g, 19.62 mmol) in CHCl3 (80 ml) at 0° C. The resulting mixture was stirred at 0° C. for 30 min. The solvent was evaporated under reduced pressure at room temperature, the residue was suspended in POCl3 (15 ml, 156.96 mmol), and PCl5 (8.2 g, 39.24 mmol) was added slowly. The reaction was stirred at 60° C. for 18 h, then cooled to room temperature and poured onto crushed ice (200 g). The aqueous mixture was extracted with CHCl3 (2×150 ml) and the combined organic layers was dried (MgSO4). The solid was removed by filtration and the filtrate was concentrated to give 3-methoxy-2-thiophenesulfonyl chloride as a brown oil (1.81 g, 43% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342610B2
Source datasetuspto-grants-2002_01
ORD IDord-02928c0e7ddf4362a9c2b4eaa6790cef
Source noteuspto-grants-2002_01