HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401435Generated: October 25, 2026
Dimethyl Sulfoxide → 2-(Trifluoromethyl)-5-(2-methyloxiran-2-yl)pyridine
https://huagongshe.com/reaction/1401435
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
DMSO is added to NaH (1-1.8 equiv.) and heated to 65° C. for 1 h. THF is added at the same temperature and heated for another 10 min. After 10 min., the reaction mixture is cooled to 0° C. Trimethylsulfonium iodide (1-1.2 equiv.) is added and the contents stirred for 10 min. after which the solution of 5-acetyl-2-(trifluoromethyl) pyridine (1 equiv.) in THF is added dropwise. After complete addition, the reaction mixture is stirred at RT for 2 h; the reaction is monitored by LCMS. After completion, the reaction mixture is poured in ice water, extracted in diethyl ether, dried over sodium sulfate and concentrated at 25° C. to get the crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08907097B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-bb7b4e39401b4ad891fdb51240d3d2bc |
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| Source note | uspto-grants-2014_12 |
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