HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287442Generated: October 31, 2026
Dimethyl Sulfoxide → HCID 10825624, compound
https://huagongshe.com/reaction/2287442
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | HCID 9881460 | HCID 9881460 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10825624 | HCID 10825624 | 90% |
Reaction Steps
A suspension of 60% NaH (876 mg, 0.022 mol) in THF (30 ml) - DMSO (50 ml) was heated to an external temperature of 50° C., followed by the addition of trimethylsulfoxonium iodide (4.8 g, 0.022 mol) in portions. After stirring at the same temperature for one hour, the reaction mixture was cooled to -20° C. and added dropwise with a solution of 2-ethylthio-2,2,2', 4'-tetrafluoroacetophenone (4.6 g, 0.018 mol) in THF (20 ml). The resulting mixture was stirred at room temperature for 2 hours. The reaction mixture was then poured into ice water, followed by extraction with ethyl acetate. The extract was washed successively with water and saturated saline and dried over magnesium sulfate. The solvent was then distilled off under reduced pressure, whereby 2-(2,4-difluorophenyl)-2-[(ethylthio) (difluoro)methyl]oxirane (4.3 g, yield: 90.0%) was obtained as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06083968 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-83c168a6d4ca40499a889bb73c187c48 |
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| Source note | uspto-grants-2000_07 |
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