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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753218Generated: October 28, 2026

5-Bromo-2-methoxy-3-methylpyridine → 6-Methoxy-5-methylnicotinonitrile

https://huagongshe.com/reaction/1753218

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-methoxy-3-methylpyridineHCID 22591176—
ReactantHCID 178418546HCID 178418546—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product6-Methoxy-5-methylnicotinonitrileHCID 5341598893%

Reaction Steps

To a solution of 5-bromo-2-methoxy-3-methyl-pyridine (1.0 g, 5.0 mmol) in DMF (10 ml) was added CuCN (0.534 g, 6.0 mmol) and the resulting mixture is heated at reflux for 28 h. After cooling to room temperature the mixture is diluted with EtOAc and washed with 10% ammonia solution followed by water and brine solution. The organic layer was separated, dried over MgSO4 and evaporated under reduced pressure. The residue was purified by flash chromatography (5% EtOAc/Hexane) to give 5-cyano-2-methoxy-3-methyl-pyridine (36) (0.68 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163020B2
Source datasetuspto-grants-2015_10
ORD IDord-3331207347604db1bc03788b882b2c3f
Source noteuspto-grants-2015_10