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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049485Generated: November 1, 2026

Isobutyronitrile → 3-(2-Bromo-5-((tert-butyl(dimethyl)silyl)oxy)phenyl)-2,2-dimethylpropanenitrile

https://huagongshe.com/reaction/1049485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyronitrileHCID 6559—
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium ChlorideHCID 25517—
Reactant(4-Bromo-3-bromomethyl-phenoxy)-tert-butyl-dimethyl-silaneHCID 19437125—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3-(2-Bromo-5-((tert-butyl(dimethyl)silyl)oxy)phenyl)-2,2-dimethylpropanenitrileHCID 131736014—

Reaction Steps

Under a nitrogen atmosphere, to a solution of diisopropylamine (0.70 mL) in THF (15 mL) was added a 1.6 M solution of n-butyllithium in hexane (3.0 mL) at 0° C., and the mixture was stirred for 10 min. Isobutyronitrile (0.47 mL) was added at −78° C., and the mixture was stirred for 30 min. A solution of (4-bromo-3-(bromomethyl)phenoxy) (tert-butyl)dimethylsilane (1.00 g) in THF (5.0 mL) was added, and the mixture was stirred at −78° C. for 2 hr. To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The extract was washed with 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 (905 mg) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382188B2
Source datasetuspto-grants-2016_07
ORD IDord-d91cb012c3f64ed79c18d91be5ed1ee9
Source noteuspto-grants-2016_07