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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854164Generated: November 2, 2026

Potassium Carbonate → (R)-2-[2-(5-Fluoro-2-methoxyphenyl)-2-methylpropyl]-2-trifluoromethyloxirane

https://huagongshe.com/reaction/854164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium BicarbonateHCID 516892—
ReactantOxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 2735153—
Reactant(S)-1,1,1-trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methyl-2-p-tolylsulfanylmethylpentan-2-olHCID 16115564—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(R)-2-[2-(5-Fluoro-2-methoxyphenyl)-2-methylpropyl]-2-trifluoromethyloxiraneHCID 1120856595%

Reaction Steps

To a solution of (S)-1,1,1-trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methyl-2-p-tolylsulfanylmethylpentan-2-ol (42.7 g, 102 mmol) in 250 mL of anhydrous dichloromethane was added trimethyloxonium tetrafluoroborate (22.7 g, 153 mmol). The resulting suspension was stirred at room temperature for 4.5 hours. A solution of potassium carbonate (42.4 g, 307 mmol) in 250 mL of water was then added. After 16 hours, the reaction mixture was poured into 200 mL of saturated aqueous sodium bicarbonate solution and extracted with three 400 mL portions of dichloromethane. The combined organic phases were washed with brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. Purification by column chromatography with silica gel (eluted with 0%-2% EtOAc/hexanes) afforded the title compound as a pale yellow oil (28.3 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256300B2
Source datasetuspto-grants-2007_08
ORD IDord-7745338889884fc8ae96258e3775bef4
Source noteuspto-grants-2007_08