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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268981Generated: October 26, 2026

Chlorosulfonic acid → 2-Ethylthieno[2,3-b]pyridine-3-sulfonyl chloride

https://huagongshe.com/reaction/2268981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPhosphorus pentachlorideHCID 24819—
Reactant2-Ethylthieno[2,3-b]pyridineHCID 12044914—
SolventDichloromethaneHCID 6344—
Product2-Ethylthieno[2,3-b]pyridine-3-sulfonyl chlorideHCID 1204491557.3%

Reaction Steps

To a solution of 2-ethylthieno[2,3-b]pyridine (0.43 g, 2.6 mmoles) in CH2Cl2 (10 ml) at −78° C. was added chlorosulfonic acid (0.9 ml, 13 mmoles). The reaction was warmed to ambient temperature over a 1 hr. period, then stirred an additional 20 hrs., followed by the addition of phosphorus oxychloride (1.7 ml, 18 mmoles) and phosphorus pentachloride (0.82 g, 4.0 mmoles). One hour later the reaction mixture was added to ice (100 ml) and extracted with EtOAc (75 ml), then washed with sat. NaHCO3 (200 ml). The organic phase was dried (MgSO4), filtered and concentrated to collect a brown oil. Flash chromatography (10% EtOAc/hexanes) provided 0.39 g (56%) of the title compound as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329387B2
Source datasetuspto-grants-2001_12
ORD IDord-632d16e2f47a473a91a2523fcd324367
Source noteuspto-grants-2001_12