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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899635Generated: November 1, 2026

Potassium Hydroxide → HCID 15453202, compound

https://huagongshe.com/reaction/1899635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 15453201HCID 15453201—
SolventMethanolHCID 887—
ProductHCID 15453202HCID 15453202101.2%

Reaction Conditions

Temperature45 °C

Reaction Steps

N-Benzenesulfonyl-N-(3-methyl-4-phenyl-5-isoxazolyl)benzenesulfonamide (300 mg, 0.66 mmol) was dissolved in methanol. Potassium hydroxide (300 mg, 5.5 mmol) was added and the solution was warmed to 45° C. to dissolve the sodium hydroxide. Stirring was continued for 20 min. Methanol was removed under reduced pressure. The residue was dissolved in water, cooled to 0° C. and acidified to pH 3-4 with concentrated HCl. The solid precipitate was extracted with ethyl acetate, dried and evaporated in vacuo to give 210 mg (100% yield) of N-(3-methyl-4-phenyl-5-isoxazolyl)benzenesulfonamide, which was further purified by recrystallization from ethyl acetate/hexanes, m.p. 124°-126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571821
Source datasetuspto-grants-1996_11
ORD IDord-b8a5199a7eeb443ab91e77e2ba830f6c
Source noteuspto-grants-1996_11