HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451490Generated: October 30, 2026
Benzoyl Peroxide → (3-Bromo-3-phenylpropoxy)(tert-butyl)dimethylsilane
https://huagongshe.com/reaction/451490
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Tert-butyldimethyl(3-phenylpropoxy)silane | HCID 10083485 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | (3-Bromo-3-phenylpropoxy)(tert-butyl)dimethylsilane | HCID 67335370 | — |
Reaction Steps
A suspension of tert-butyldimethyl(3-phenylpropoxy)silane (2.22 g, 8.86 mmol), N-bromosuccinimide (1.58 g, 8.86 mmol) and benzoyl peroxide (66.4 mg, 266 μmol) in carbon tetrachloride (17.8 mL) was heated to reflux for 3 hours. The reaction was filtered, the precipitate washed with carbon tetrachloride and the solvent was evaporated. Water was added and the reaction was extracted twice with diethyl ether. The combined organic layers were washed with saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and the solvent was evaporated under reduced pressure. The title compound was obtained as a light yellow oil (1.63 g, 55%) after column chromatography on silica gel using heptane/ethyl acetate 19:1 (v/v) as eluent. 1H NMR (CDCl3, 300 MHz): δ (ppm)=7.42-7.26 (m, 5H), 5.42 (dd, 1H), 3.76 (m, 1H), 3.68 (m, 1H), 2.48 (m, 1H), 2.28 (m, 1H), 0.90 (s, 9H), 0.06 (s, 3H), 0.03 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486967B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-adf8ea6fa3bf4ff4ad7f77e4ab8d39c9 |
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| Source note | uspto-grants-2013_07 |
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