HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129371Generated: October 25, 2026
Hydrogen Peroxide → 1-Cyclohexylsulfonyl-3,3-dimethyl-2-butanone
https://huagongshe.com/reaction/129371
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Cyclohexanethiol | HCID 15290 | — |
| Reactant | Bromopinacolone | HCID 21642 | — |
| Catalyst | Sodium tungstate | HCID 26052 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Cyclohexylsulfonyl-3,3-dimethyl-2-butanone | HCID 22908632 | 28.7% |
Reaction Steps
To cyclohexylthiol (23 g, 0.198 mole), a solution of potassium hydroxide (13.7 g, 0.207 mole) in ethanol (80 ml) was added dropwise at 15° C., followed by stirring at the same temperature for 24 hours. After 1-bromo-3,3-dimethyl-2-butanone (35.4 g, 0.198 mole) was added dropwise to the reaction mixture at 10°-15° C. and continued to stir at 20° C. for 5 hours, sodium tungstate (2.5 g) was added. Then, 30% hydrogen peroxide (220 g, 1.96 mole) was added dropwise at 45°-50° C. and reacted with stirring at 60°-80° C. for 30 hours. After cooling, the reaction mixture was extracted with methylene chloride (300 ml×1), the organic layer was separated, dried over anhydrous MgSO4 and evaporated to obtain 14 g of residual crude 1-cyclohexylsulfonyl-3,3-dimethyl-2-butanone as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05468589 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-5f9e35a15e6347eb878ff043c31f1985 |
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| Source note | uspto-grants-1995_11 |
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