Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842891Generated: October 30, 2026

Sodium Hydroxide → HCID 18617352, compound

https://huagongshe.com/reaction/842891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 18617325HCID 18617325—
SolventMethanolHCID 887—
ProductHCID 18617352HCID 18617352—

Reaction Conditions

Temperature25 °C

Reaction Steps

Sodium hydroxide (1.3 g, 30.6 mmol) was added to a solution of N-(benzenesulfonyl)-N-(4-bromo-5-methyl-3-isoxazolyl)benzene-sulfonamide (7g, 15.3 mmol, prepared as described in (a)) in methanol (100 ml). The resulting solution was stirred at 25° C. for 30 h. Excess methanol was removed under reduced pressure. The residue was dissolved in water (50 ml) and acidified (pH 3-4)by the addition of concentrated HCl with cooling. The mixture was extracted with dichloromethane (2×100 ml) and the combined organic layer was dried over anhydrous magnesium sulfate. Removal of the solvent gave N-(4-bromo-5-methyl-3-isoxazolyl)benzenesulfonamide which was purified by crystallization from ethyl acetate/hexanes (4.5 g, 92% yield). The compound is identical to the one isolated in step (b).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376523B1
Source datasetuspto-grants-2002_04
ORD IDord-443981e63bb14d668959d6752695fc3e
Source noteuspto-grants-2002_04