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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Trimethylsulfonium iodide | HCID 75127 | — |
| Reactant | 1-[6-(Trifluoromethyl)pyridin-3-yl]ethan-1-one | HCID 21880578 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Trifluoromethyl)-5-(2-methyloxiran-2-yl)pyridine | HCID 59454978 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409910B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-327acde6ca5e4f81a692f2036fd2b88c |
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| Source note | uspto-grants-2016_08 |
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