HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845565Generated: October 30, 2026
Tetrahydrofuran → HCID 20131574, compound
https://huagongshe.com/reaction/845565
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | HCID 13021647 | HCID 13021647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 20131574 | HCID 20131574 | 32.1% |
Reaction Steps
A mixture of 20 g of 1-fluoro-1-(1H-1,2,4-triazol-1-yl)-3,3-dimethyl-2-butanone, 13.5 g of potassium tertiary butylate, 24.0 g of trimethylsulfoxonium iodide, 80 ml of tetrahydrofuran and 20 ml of dimethyl sulfoxide is stirred at 60° C. for 6 hours. The reaction mixture is then 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. Crystallisation from petroleum ether gives 6.9 g of 2-tert.-butyl-2-[(1H-1,2,4-triazol-1-yl)-fluoromethyl]-oxirane, melting point 72°-74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04758670 |
|---|
| Source dataset | uspto-grants-1988_07 |
|---|
| ORD ID | ord-744359229e0f4e64b37728f849fedf63 |
|---|
| Source note | uspto-grants-1988_07 |
|---|