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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398282Generated: October 30, 2026

Furan → Furan-2-sulfonyl Chloride

https://huagongshe.com/reaction/398282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFuranHCID 8029—
ReactantChlorosulfonic acidHCID 24638—
ReactantPhosphorus pentachlorideHCID 24819—
ProductFuran-2-sulfonyl ChlorideHCID 27950728.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Phosphorus pentachloride (15.29 g, 73.44 mmol) was added portionwise (caution, foaming) over 5 min at 0° C. to chlorosulfonic acid (21.39 g, 183.6 mmol) and the resulting solution was stirred at 0° C. for 10 min. Then, furan (5.0 g, 73.44 mmol) was added in one portion and the resulting dark suspension was stirred at 0° C. for 15 min during which time foaming occurred and subsided. The reaction mixture was then poured onto ice and the resulting suspension was extracted with CH2Cl2 (150 mL). The organic extract was filtered through a pad of celite, washed with brine and dried over MgSO4. The solvent was removed in vacuo to provide 2-furansulfonyl chloride as a black oil (1.01 g, 7.9%). 1H-NMR (DMSO-d6, 400 MHz) δ7.4 (d, 1H); 6.38 (d, 1H); 6.35 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610734B2
Source datasetuspto-grants-2003_08
ORD IDord-803c3cf65af6429dbfaf1754a5f882ad
Source noteuspto-grants-2003_08