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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309322Generated: November 1, 2026

Ammonium Hydroxide → 2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-sulfonamide

https://huagongshe.com/reaction/2309322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-sulfonyl chlorideHCID 13424179—
SolventTetrahydrofuranHCID 8028—
Product2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-sulfonamideHCID 13424180—

Reaction Steps

A solution of 26 g of 2,3-dihydro-2,2-dimethyl-7-benzofuransulfonyl chloride prepared in Example 1, in 130 ml of tetrahydrofuran, was cooled in an ice-water bath while about 30 ml of concentrated aqueous ammonium hydroxide was added portionwise at 10° to 30° C. The resulting suspension was stirred at room temperature for 3 hours, then the solvent was evaporated under reduced pressure. The residue was stirred in 150 ml of water for 0.5 hour, then filtered. The crude, wet solid was dissolved in chloroform and dried over sodium sulfate. The solvent was evaporated under reduced pressure to give a dry solid. The solid was washed once with about 100 ml of hot toluene to give 20 g of 2,3-dihydro-2,2-dimethyl-7-benzofuransulfonamide, m.p. 163°-165° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04695310
Source datasetuspto-grants-1987_09
ORD IDord-852913dcb9e9433a817c1e572a564c83
Source noteuspto-grants-1987_09