HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → 2-Benzyloxy-6-cyano-3-methylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Bromo-5-methylpyridine-2-carbonitrile | HCID 21928322 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Benzyloxy-6-cyano-3-methylpyridine | HCID 21928305 | 52% |
Reaction Steps
To a solution of 2-bromo-6-cyano-3-methylpyridine (272 mg) and benzyl alcohol (156 mg) in tetrahydrofuran (20 mL) was added sodium hydride (40 mg), and the mixture was heated under reflux for one hour. The reaction mixture was cooled to room temperature, diluted with ethyl acetate, washed successively with saturated aqueous sodium bicarbonate and saturated brine, and dried over anhydrous sodium sulfate. After removal of the sodium sulfate by filtration, the organic solvent was evaporated off in vacuo. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=19:1) to give the title compound (161 mg) as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07119107B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-049107b3004541678c41d2d7cd3017b8 |
| Source note | uspto-grants-2006_10 |