HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 5-Phenylpyridine-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 5-Bromopyridine-2-carbonitrile | HCID 817154 | — |
| Catalyst | HCID 178420430 | HCID 178420430 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Phenylpyridine-2-carbonitrile | HCID 935276 | 136.7% |
Reaction Steps
A mixture comprising 5-bromopyridine-2-carbonitrile (0.09 g, 0.49 mmol), phenyl boronic acid (0.12 g, 0.98 mmol), 2M sodium carbonate ((0.98 mL, 1.96 mmol), tetrakis(tritylphosphanyl)palladium (0.06 g, 0.049 mmol), benzene (2 mL) and ethanol (2 mL) was heated at reflux for 1 hour and then partitioned between ethyl acetate and water. The organic layer was separated, washed with water, dried (MgSO4) and concentrated. The residue was purified by silica gel chromatography (25% ethyl acetate/hexanes) to provide 5-phenylpyridine-2-carbonitrile (0.12 g, 0.67 mmol). MS (CI), Calculated for C12H8N2, 180.2, Found (MH+): 182.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06150379 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-96de982658ac4e01a4410be3ef68cd39 |
| Source note | uspto-grants-2000_11 |