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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481393Generated: October 25, 2026

Dimethyl Sulfoxide → 2-(Trifluoromethyl)-5-(2-methyloxiran-2-yl)pyridine

https://huagongshe.com/reaction/1481393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
ReactantTrimethylsulfonium iodideHCID 75127—
Reactant1-[6-(Trifluoromethyl)pyridin-3-yl]ethan-1-oneHCID 21880578—
SolventTetrahydrofuranHCID 8028—
Product2-(Trifluoromethyl)-5-(2-methyloxiran-2-yl)pyridineHCID 59454978—

Reaction Conditions

Temperature65 °C

Reaction Steps

The title compound was prepared by following general procedure 3. DMSO was added to NaH (1 equiv.) and heated to 65° C. for 1 h. THF was added at the same temperature and heated for another 10 min. After 10 min., the reaction mixture was cooled to 0° C. Trimethylsulfonium iodide (1 equiv.) was added and stirred for 10 min. after which the solution of 1-(6-(trifluoromethyl)pyridin-3-yl)ethanone (1 equiv.) in THF was added dropwise. After complete addition, the reaction mixture was stirred at RT for 2 h. The product was detected by LCMS and the reaction mixture was poured into ice water, extracted in diethyl ether (4×50 mL), dried over Na2SO4 and concentrated at 25° C. to obtain the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409910B2
Source datasetuspto-grants-2016_08
ORD IDord-327acde6ca5e4f81a692f2036fd2b88c
Source noteuspto-grants-2016_08