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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202233Generated: October 31, 2026

Acetonitrile → 2-(6-Methoxypyridin-2-yl)acetonitrile

https://huagongshe.com/reaction/2202233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant2-Bromo-6-methoxypyridineHCID 256810—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product2-(6-Methoxypyridin-2-yl)acetonitrileHCID 4548986458%

Reaction Conditions

Temperature-78 °C

Reaction Steps

1.6M n-Butyllithium/hexane solution (300 mL, 479.43 mmol) was added to a solution of acetonitrile (21.87 g, 532.70 mmol) in THF (630 mL) at −78° C. under argon atmosphere, and the mixture was stirred at −78° C. for 30 min. 2-Bromo-6-methoxypyridine (25.04 g, 133.18 mmol) was added dropwise thereto over 15 min at −78° C., and the reaction mixture was stirred at room temperature for 4 hr. The reaction mixture was poured into ice water (900 mL), and the mixture was extracted with ethyl acetate (×3). The organic layer was washed with water and brine, and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 2→20% ethyl acetate/hexane) to give 2-(6-methoxypyridin-2-yl)acetonitrile (11.37 g, 77 mmol, 58%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365520B2
Source datasetuspto-grants-2016_06
ORD IDord-261c817bcb0f409b93eb8660436bb3f8
Source noteuspto-grants-2016_06