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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049484Generated: October 30, 2026

Azobisisobutyronitrile → (4-Bromo-3-bromomethyl-phenoxy)-tert-butyl-dimethyl-silane

https://huagongshe.com/reaction/1049484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant(4-Bromo-3-methylphenoxy)(tert-butyl)dimethylsilaneHCID 17984598—
SolventEthyl AcetateHCID 8857—
Product(4-Bromo-3-bromomethyl-phenoxy)-tert-butyl-dimethyl-silaneHCID 1943712530.1%

Reaction Steps

To a solution of (4-bromo-3-methylphenoxy)(tert-butyl)dimethylsilane (6.97 g) and N-bromosuccinimide (6.21 g) in ethyl acetate (100 mL) was added 2,2′-azobis(isobutyronitrile) (383 mg), and the mixture was refluxed for 17 hr. The mixture was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (2.65 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382188B2
Source datasetuspto-grants-2016_07
ORD IDord-3757b5f31c3541aba121606f57cb3e81
Source noteuspto-grants-2016_07