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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 129371생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물Potassium HydroxideHCID 14797—
반응물CyclohexanethiolHCID 15290—
반응물BromopinacoloneHCID 21642—
촉매Sodium tungstateHCID 26052—
용매EthanolHCID 702—
생성물1-Cyclohexylsulfonyl-3,3-dimethyl-2-butanoneHCID 2290863228.7%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05468589
출처 데이터셋uspto-grants-1995_11
ORD IDord-5f9e35a15e6347eb878ff043c31f1985
출처 메모uspto-grants-1995_11