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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789127Generated: November 1, 2026

Tetrahydrofuran → HCID 13472236, compound

https://huagongshe.com/reaction/1789127

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 numberUS04687508
Source datasetuspto-grants-1987_08
ORD IDord-1b8604044755497b8d713cda5a70a3fa
Source noteuspto-grants-1987_08