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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089892Generated: October 31, 2026

Hydrogen Peroxide → HCID 14403426, compound

https://huagongshe.com/reaction/1089892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
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) of dimethyl sulphide and 32.5 g (0.26 mol) of dimethyl sulphate are added to 40 ml of tert.-butanol and the mixture is 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 is initially added dropwise to the reaction mixture with stirring and 29.2 g of potassium hydroxide powder are then introduced, the temperature of the reaction mixture being held at 20° to 30° C. The mixture is stirred for a further 3 hours at 30° C., then the dimethyl sulphide is stripped off 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 using water and concentrated by stripping off 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 further reacted without additional purification. ##STR72##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05079374
Source datasetuspto-grants-1992_01
ORD IDord-d49ad6948d844f49b7280740eeae1a77
Source noteuspto-grants-1992_01