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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287442Generated: October 31, 2026

Dimethyl Sulfoxide → HCID 10825624, compound

https://huagongshe.com/reaction/2287442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
ReactantHCID 9881460HCID 9881460—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10825624HCID 1082562490%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06083968
Source datasetuspto-grants-2000_07
ORD IDord-83c168a6d4ca40499a889bb73c187c48
Source noteuspto-grants-2000_07