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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854167Generated: October 30, 2026

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

https://huagongshe.com/reaction/854167

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-methylphenyl)-4-methyl-2-p-tolylsulfanylmethylpentan-2-olHCID 58933188—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(R)-2-[2-(5-Fluoro-2-methylphenyl)-2-methylpropyl]-2-trifluoromethyloxiraneHCID 1170181278%

Reaction Steps

To a solution of (S)-1,1,1-trifluoro-4-(5-fluoro-2-methylphenyl)-4-methyl-2-p-tolylsulfanylmethylpentan-2-ol (1.37 g, 3.41 mmol) in 10 mL of anhydrous dichloromethane was added trimethyloxonium tetrafluoroborate (757 mg, 5.12 mmol). The resulting suspension was stirred at room temperature for 4.5 hours. A solution of potassium carbonate (1.41 g, 10.2 mmol) in 10 mL of water was then added. After 19 hours, the reaction mixture was poured into 40 mL of saturated aqueous sodium bicarbonate solution and extracted with three 50 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 clear oil (731 mg, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256300B2
Source datasetuspto-grants-2007_08
ORD IDord-9b666b83b16d4b96b05a745eaec8e9af
Source noteuspto-grants-2007_08