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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantTert-butyldimethyl(3-phenylpropoxy)silaneHCID 10083485—
SolventCarbon TetrachlorideHCID 5943—
Product(3-Bromo-3-phenylpropoxy)(tert-butyl)dimethylsilaneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486967B2
Source datasetuspto-grants-2013_07
ORD IDord-adf8ea6fa3bf4ff4ad7f77e4ab8d39c9
Source noteuspto-grants-2013_07