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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483055Generated: October 30, 2026

Tetrahydrofuran → HCID 13472236, compound

https://huagongshe.com/reaction/483055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium HydroxideHCID 14923—
ReactantSulfuryl chlorideHCID 24648—
ProductHCID 13472236HCID 13472236—

Reaction Steps

A solution of 9.8 g of the sulfonyl chloride, prepared in Part A, in 150 ml tetrahydrofuran was cooled to approximately 5°, and 6.6 ml of concentrated ammonium hydroxide was added dropwise. The resulting yellow suspension was allowed to warm to ambient temperature and stirred 0.5 hour; thin-layer chromatography showed the reaction was complete. The solvent was evaporated in vacuo and the resulting solid was slurried in 150 ml water, collected, washed with water and dried. The crude product was washed with 1-chlorobutane and dried to give 7.74 g of 1,3-dihydrobenzo[c]furan-4-sulfonamide, m.p. 153°-158°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04578108
Source datasetuspto-grants-1986_03
ORD IDord-150e1381f12541dfb9d8be5ded0788fc
Source noteuspto-grants-1986_03