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HRID 241465作成日:2026年10月27日

Hydrogen Peroxide → 1-Methyl-1-phenylundecyl hydroperoxide

https://huagongshe.com/reaction/241465

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物TetrahydrofuranHCID 8028—
反応物2-Phenyl-2-bromododecaneHCID 67084407—
触媒Silver trifluoroacetateHCID 76299—
溶媒Sodium BicarbonateHCID 516892—
生成物1-Methyl-1-phenylundecyl hydroperoxideHCID 86643019—

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08650742B2
出典データセットuspto-grants-2014_02
ORD IDord-0d011dcd27524acc9b0ac7e4ad0d3f9c
出典メモuspto-grants-2014_02