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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269625Generated: November 1, 2026

Methanol → 2-(Methylsulfonyl)-4-[4-(trifluoromethyl)phenyl]pyrimidine

https://huagongshe.com/reaction/1269625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-Methylsulfanyl-4-(4-trifluoromethylphenyl)pyrimidineHCID 18448355—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventWaterHCID 962—
Product2-(Methylsulfonyl)-4-[4-(trifluoromethyl)phenyl]pyrimidineHCID 18448354—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 2-(methylthio)-4-[4-(trifluoromethyl)phenyl]pyrimidine (2.24 g, 8.4 mmol) in methanol (85 mL) and water (85 mL) at 0° C. was added oxone™ (15.25 g, 24.8 mmol). The reaction was stirred at 0° C. for 1 h and then at room temperature for 18 h. The reaction mixture was diluted with water (200 mL) and extracted with chloroform (2×250 mL). The organic solution was dried (Na2SO4) filtered and evaporated to afford the title compound as a white solid (2.235 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199239B2
Source datasetuspto-grants-2007_04
ORD IDord-59ca30d8c1cc4c139472372c9ce1e541
Source noteuspto-grants-2007_04