Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium HydroxideHCID 14797—
ReactantCyclohexanethiolHCID 15290—
ReactantBromopinacoloneHCID 21642—
CatalystSodium tungstateHCID 26052—
SolventEthanolHCID 702—
Product1-Cyclohexylsulfonyl-3,3-dimethyl-2-butanoneHCID 2290863228.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468589
Source datasetuspto-grants-1995_11
ORD IDord-5f9e35a15e6347eb878ff043c31f1985
Source noteuspto-grants-1995_11