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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838509Generated: October 26, 2026

Potassium peroxymonosulphate → 4-[3,5-Difluoro-4-(methylsulfonyl)-phenyl]-5-methyl-3-phenylisoxazole

https://huagongshe.com/reaction/1838509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium peroxymonosulphateHCID 10313463—
ReactantMagnesium 2-(dioxidan-2-ide-1-carbonyl)benzoate--water (1/1/6)HCID 21894687—
Reactant4-[3,5-Difluoro-4-(methylsulfinyl)phenyl]-5-methyl-3-phenylisoxazoleHCID 22745613—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-[3,5-Difluoro-4-(methylsulfonyl)-phenyl]-5-methyl-3-phenylisoxazoleHCID 992448993.5%

Reaction Steps

Potassium peroxymonosulfate (0.25 g, 0.40 mmol) and water (7 mL) were added to a mixture of 4-[3,5-difluoro-4-(methyl-sulfinyl)phenyl]-5-methyl-3-phenylisoxazole (0.10 g, 0.30 mmol), dichloromethane (4 mL), and methanol (4 mL). The mixture was stirred for four days at room temperature. To the mixture was added magnesium monoperoxyphathalate hexahydrate (0.50 g, 0.80 mmol), dichloromethane (20 mL), methanol (10 mL). The mixture was stirred vigorously for 18 hours. To the mixture was added potassium peroxymonosulfate (0.35 g, 0.57 mmol), and the reaction continued for 18 hours. The mixture was poured into water and extracted with dichloromethane (4×75 mL). The combined extracts were dried with magnesium sulfate, concentrated, and the residue purified by silica gel chromatography using 30% ethyl acetate in hexanes. A white solid (98 mg, 93%) was obtained. MP 140.4-143.4° C. 1H NMR (CDCl3/400 MHz) 7.35-7.45 (m, 5H), 6.84 (d, 2H, J=9.4), 3.32 (s, 3H) 2.52 (s, 3H). ESHRMS m/z 350.0642 (M+H+, Calcd 350.0662).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673818B2
Source datasetuspto-grants-2004_01
ORD IDord-4ccb8b5256d64cf58457e0492844e8a5
Source noteuspto-grants-2004_01