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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650729Generated: November 1, 2026

Dimethyl Sulfide → HCID 14403426, compound

https://huagongshe.com/reaction/1650729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantDimethyl SulfateHCID 6497—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 14403425HCID 14403425—
Solventtert-ButanolHCID 6386—
ProductHCID 14403426HCID 1440342682%

Reaction Steps

21 ml (0.29 mol) o& dimethyl sulphide and 32.5 g (0.26 mol) of dimethyl sulphate are added to 40 ml of tert.-butanol and allowed to stand at room temperature for 14 hours. A solution of 30 g (0.095 mol) of 4-chlorophenylethyl 1-phenylmercapto-cyclopropyl ketone in 90 ml of tert.-butanol are first added dropwise to the reaction mixture with stirring and 29.2 g of potassium hydroxide powder are then introduced, while the temperature of the reaction mixture is held at 20 to 30° C. The mixture is stirred for a further 3 hours at 30° C., then the dimethyl sulphide is removed under reduced pressure and the reaction mixture is then poured into 70 ml of a 1% strength aqueous hydrogen peroxide solution. The mixture is extracted with ethyl acetate. The organic phase is washed with water and concentrated by removing the solvent under reduced pressure after drying over sodium sulphate. In this manner, 25.6 g (82% of theory) of 2-(4-chlorophenylethyl)-2-(1-phenylmercapto-cyclopropyl)oxirane are obtained in the form of an oily product which is reacted further without additional purification. ##STR68##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925865
Source datasetuspto-grants-1990_05
ORD IDord-fc1e29bcfb8645a1b8463a663c5c6c66
Source noteuspto-grants-1990_05