HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946214Generated: October 26, 2026
Bromotrimethylsilane → 2-Phenyl-2-bromododecane
https://huagongshe.com/reaction/1946214
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | 1-Methyl-1-phenylundecyl alcohol | HCID 65147666 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Phenyl-2-bromododecane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399049B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-13c2d51b0d8a41baafdd17cd92697087 |
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| Source note | uspto-grants-2013_03 |
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