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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193442Generated: October 31, 2026

Ammonium Hydroxide → 2-(5-Isoxazolyl)benzenesulfonamide

https://huagongshe.com/reaction/1193442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant2-(isoxazol-5-yl)benzene-1-sulfonyl chloride(WXC09362)HCID 13489811—
SolventTetrahydrofuranHCID 8028—
Product2-(5-Isoxazolyl)benzenesulfonamideHCID 13489813—

Reaction Steps

A solution of 37 g of 2-(isoxazol-5-yl)benzenesulfonyl chloride, prepared in Example 4, in 200 ml of tetrahydrofuran, was cooled in an ice-water bath while about 40 ml of concentrated aqueous ammonium hydroxide was added slowly at 10° to 30° C. The resulting suspension was stirred at room temperature for 4 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 tetrahydrofuran and dried over sodium sulfate. The solid was recrystallized from 2-propanol to give 20 g of the title compound; m.p. 132°-135° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04810282
Source datasetuspto-grants-1989_03
ORD IDord-406e38c8c6fd4f68a6e0e1f291903469
Source noteuspto-grants-1989_03