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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 241465생성일: 2026년 10월 26일

Hydrogen Peroxide → 1-Methyl-1-phenylundecyl hydroperoxide

https://huagongshe.com/reaction/241465

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물TetrahydrofuranHCID 8028—
반응물2-Phenyl-2-bromododecaneHCID 67084407—
촉매Silver trifluoroacetateHCID 76299—
용매Sodium BicarbonateHCID 516892—
생성물1-Methyl-1-phenylundecyl hydroperoxideHCID 86643019—

반응 단계

10.50 g (0.04 mol) of 1-methyl-1-phenylundecyl alcohol was dissolved in 50 ml of dichloromethane, cooled in ice bath, 10.6 ml (12.29 g, 0.08 mol) of trimethylsilyl bromide was added and the mixture stirred for 1 h under protection from moisture. The solution was diluted with 100 ml ether and washed four times with 50 ml water, brine, dried and evaporated to give crude 2-phenyl-2-bromododecane. 35 ml of 2.3 M hydrogen peroxide in THF (0.08 mol) was added to the 2-phenyl-2-dodecyl bromide and the mixture was cooled on ice bath. 8.84 g (0.04 mol) of silver trifluoroacetate was added. 70 ml of conc. NaHCO3 was added and the mixture filtered. The reaction flask and the filter cake was rinsed with diethyl ether. The aqueous phase was separated and the organic phase washed with conc. NaHCO3, 50 ml water, brine, dried and evaporated to give an oil. The oil was purified by flash chromatography using 2:8 ether:pentane as eluent. The yield of 1-methyl-1-phenylundecyl hydroperoxide was 30%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08650742B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-0d011dcd27524acc9b0ac7e4ad0d3f9c
출처 메모uspto-grants-2014_02