HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703349Generated: October 29, 2026
Hydrogen Peroxide → HCID 14403426, compound
https://huagongshe.com/reaction/703349
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 14403425 | HCID 14403425 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 14403426 | HCID 14403426 | 82% |
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. ##STR73##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983208 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-2d1cd5a7abd44ba0aac6f3ef5d3cb8ae |
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| Source note | uspto-grants-1991_01 |
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