Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 129371Erstellt: 23. Oktober 2026

Hydrogen Peroxide → 1-Cyclohexylsulfonyl-3,3-dimethyl-2-butanone

https://huagongshe.com/de/reaction/129371

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktPotassium HydroxideHCID 14797—
EduktCyclohexanethiolHCID 15290—
EduktBromopinacoloneHCID 21642—
KatalysatorSodium tungstateHCID 26052—
LösungsmittelEthanolHCID 702—
Produkt1-Cyclohexylsulfonyl-3,3-dimethyl-2-butanoneHCID 2290863228,7%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05468589
Quelldatensatzuspto-grants-1995_11
ORD IDord-5f9e35a15e6347eb878ff043c31f1985
Quellennotizuspto-grants-1995_11