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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264375Generated: October 30, 2026

Sodium Cyanide → 2-(6-Bromopyridin-2-yl)acetonitrile

https://huagongshe.com/reaction/2264375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
Reactant2-Bromo-6-(bromomethyl)pyridineHCID 12954796—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2-(6-Bromopyridin-2-yl)acetonitrileHCID 64286440.8%

Reaction Steps

To a stirred solution of the above crude 6-bromo-2-bromomethylpyridine (70 g, 0.28 mol) in dioxane (500 mL) and water (250 mL), was added NaCN (28 g, 0.74 mol) at 0° C. and then stirred at RT for 16 h. The reaction mixture was quenched with 3 Lit of water and extracted with ethylacetate (4×500 mL). The organic layer was washed with water (400 L), brine (250 mL), dried over Na2SO4 and concentrated to give crude product. The crude was purified by column chromatography over silica gel (pet. ether/ethylacetate, 8:2) to give 6-bromopyridine-2-yl-acetonitrile (22.5 g, 40%). [TLC: Pet. ether/ethylacetate, 7:3, Rf=0.35]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855212B2
Source datasetuspto-grants-2010_12
ORD IDord-f7899f1205f7410e8b75a093342fbfed
Source noteuspto-grants-2010_12