HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845568Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 20131577, compound
https://huagongshe.com/reaction/845568
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | HCID 20131579 | HCID 20131579 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20131577 | HCID 20131577 | 46.9% |
Reaction Steps
12.0 g of 2-fluoro-2-(1H-1,2,4-triazol-1-yl)-4,4-dimethyl-3-pentanone are added dropwise to a mixture of 13.2 g of trimethylsulfoxonium iodide, 7.3 g of potassium tertiary butylate, 20 ml of dimethyl sulfoxide and 80 ml of tetrahydrofuran, and the reaction mixture is stirred for 18 hours at 80° C. After cooling, the mixture is taken up in ice water and extracted with ethyl acetate. The combined organic phases are washed with water and saturated sodium chloride solution, dried over sodium sulfate and evaporated. Distillation of the oily residue gives 6 g 2-tert.-butyl-2-[1-fluoro-1-(1H-1,2,4-triazol-1-yl)-ethyl]-oxirane, boiling point 60°-61° C./0.013 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04758670 |
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| Source dataset | uspto-grants-1988_07 |
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| ORD ID | ord-752d225d6a9e470d9da412860e8bea50 |
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| Source note | uspto-grants-1988_07 |
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