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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842884Generated: October 30, 2026

Sodium Hydroxide → N-(4-bromo-3-tert-butyl-5-isoxazolyl)benzenesulfonamide

https://huagongshe.com/reaction/842884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantN-Benzenesulfonyl-N-(4-bromo-3-tert-butyl-5-isoxazolyl) benzenesulfonamideHCID 18617308—
SolventMethanolHCID 887—
ProductN-(4-bromo-3-tert-butyl-5-isoxazolyl)benzenesulfonamideHCID 1861730694%

Reaction Conditions

Temperature45 °C

Reaction Steps

N-Benzenesulfonyl-N-(4-bromo-3-tert-butyl-5-isoxazolyl)benzenesulfonamide (80 mg, 0.16 mmol) was dissolved in methanol (2 ml). Sodium hydroxide (0.120 g, 3.0 mmol) in methanol was added and the solution was stirred at 45° C. 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 hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated in vacuo to give N-(4-bromo-3-tert-butyl-5-isoxazolyl)benzenesulfonamide in 94% yield. Further purification was achieved by recrystallization from methanol/water, giving an off white solid, m.p. 108-109° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376523B1
Source datasetuspto-grants-2002_04
ORD IDord-507a05a21b9a46feb2973cffdae4b457
Source noteuspto-grants-2002_04