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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384047Generated: October 30, 2026

Isobutyronitrile → 2-(6-Bromopyridin-2-yl)-2-methylpropanenitrile

https://huagongshe.com/reaction/384047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyronitrileHCID 6559—
Reactant2,6-DibromopyridineHCID 12274—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product2-(6-Bromopyridin-2-yl)-2-methylpropanenitrileHCID 5796965865.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Potassium bis(trimethylsilyl)amide (0.5 M in toluene, 200 ml, 100 mmol) was added slowly to a solution of isobutyronitrile (8.55 ml, 95.26 mmol) in toluene (200 ml) cooled down to 0° C. After complete addition, the reaction mixture was allowed to warm up to room temperature over 1 hour. The resulting mixture was added to a solution of 2,6-dibromopyridine (56.42 g, 238.15 mmol) in toluene (100 ml). The reaction mixture was stirred at room temperature for 18 hours. The crude mixture was diluted with ether, washed with a saturated aqueous solution of ammonium chloride and brine. The organic phase was dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified on silica gel by flash column chromatography to afford the title compound as an oil (14.04 g, 65% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367697B2
Source datasetuspto-grants-2013_02
ORD IDord-ccc80749565e4d3a8e5cc79fee5e0763
Source noteuspto-grants-2013_02