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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Cyanophenylboronic acid | HCID 2734325 | — |
| Reactant | 3-Bromo-6-methoxy-2-methylpyridine | HCID 10798146 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(6-Methoxy-2-methylpyridin-3-yl)benzonitrile | HCID 67492316 | 61% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173682B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-53f2c18e32ef496485cad58d7c578025 |
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| Source note | uspto-grants-2012_05 |
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