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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233584Generated: November 1, 2026

Hydrogen Peroxide → HCID 135961987, compound

https://huagongshe.com/reaction/2233584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 135961981HCID 135961981—
SolventTetrahydrofuranHCID 8028—
ProductHCID 135961987HCID 135961987—

Reaction Steps

To a solution of 50 mg of 3-{4-[4-but-3-enyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-2-chloro-phenyl}-4H-[1,2,4]oxadiazol-5-one in 2 ml of tetrahydrofuran at 0° C. was added 0.3 ml of a 2M solution of borane-methylsulfide complex in tetrahydrofuran. The resulting mixture was stirred allowing it to warm up to room temperature than stirred at room temperature for 30 minutes. After cooling to 0° C., 0.1 ml of a 5M aqueous solution of sodium hydroxide and 0.1 ml of a 30% aqueous solution of hydrogen peroxide were added. The resulting mixture was stirred allowing it to warm up to room temperature over 1 hour. It was then poured into water, extracted with ethyl acetate, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel (gradient of dichloromethane/methanol from 100/0 to 95/5) followed by crystallization from dichloromethane/pentane to give 28 mg of 3-{2-chloro-4-[4-(4-hydroxy-butyl)-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-phenyl}-4H-[1,2,4]oxadiazol-5-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709509B2
Source datasetuspto-grants-2010_05
ORD IDord-58c5e5eb5e8541a2918ba41a3513fc9c
Source noteuspto-grants-2010_05