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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845565Generated: October 30, 2026

Tetrahydrofuran → HCID 20131574, compound

https://huagongshe.com/reaction/845565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
ReactantHCID 13021647HCID 13021647—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 20131574HCID 2013157432.1%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04758670
Source datasetuspto-grants-1988_07
ORD IDord-744359229e0f4e64b37728f849fedf63
Source noteuspto-grants-1988_07