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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946215Generated: October 25, 2026

Hydrogen Peroxide → 1-Methyl-1-phenylundecyl hydroperoxide

https://huagongshe.com/reaction/1946215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantTetrahydrofuranHCID 8028—
Reactant2-Phenyl-2-bromododecaneHCID 67084407—
CatalystSilver trifluoroacetateHCID 76299—
SolventSodium BicarbonateHCID 516892—
Product1-Methyl-1-phenylundecyl hydroperoxideHCID 86643019—

Reaction Steps

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%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399049B2
Source datasetuspto-grants-2013_03
ORD IDord-cfe1651948114d77b88015c22b34e4b3
Source noteuspto-grants-2013_03