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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946214Generated: October 26, 2026

Bromotrimethylsilane → 2-Phenyl-2-bromododecane

https://huagongshe.com/reaction/1946214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromotrimethylsilaneHCID 76113—
Reactant1-Methyl-1-phenylundecyl alcoholHCID 65147666—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product2-Phenyl-2-bromododecaneHCID 67084407—

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-13c2d51b0d8a41baafdd17cd92697087
Source noteuspto-grants-2013_03