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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921324Generated: November 1, 2026

Toluene → 3-(6-Methoxy-2-methylpyridin-3-yl)benzonitrile

https://huagongshe.com/reaction/1921324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant3-Cyanophenylboronic acidHCID 2734325—
Reactant3-Bromo-6-methoxy-2-methylpyridineHCID 10798146—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventMethanolHCID 887—
Product3-(6-Methoxy-2-methylpyridin-3-yl)benzonitrileHCID 6749231661%

Reaction Steps

To a nitrogen flushed mixture of 3-cyanophenylboronic acid (5.0 g, 34 mmol), 3-bromo-6-methoxy-2-methylpyridine (4.6 g, 22.7 mmol) and palladium tetrakis(triphenylphosphine) (789 mg, 0.68 mmol) is added toluene (150 mL), methanol (12 mL) and sodium carbonate (22.7 mmol) and the mixture is heated overnight at reflux. The cooled reaction is concentrated and the residue is purified by chromatography eluting with cyclohexane-3.2 to 9% ethyl acetate. Product containing fractions are combined and concentrated to afford 3-(6-methoxy-2-methylpyridin-3-yl)benzonitrile (3.09 g, 61% yield) as a white solid. LC/MS: MS m/e=225 (M+H); RT 3.58 min; 1H NMR (CDCl3, δ ppm) 7.65 (1H, m), 7.60 (1H, m), 7.56 (2H, m), 7.40 (1H, d), 6.63 (1H, d), 3.98 (3H, s), 2.40 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173682B2
Source datasetuspto-grants-2012_05
ORD IDord-53f2c18e32ef496485cad58d7c578025
Source noteuspto-grants-2012_05