HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorobenzonitrile → 4-[2-(6-Methyl-2-pyridyl)ethoxy]benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorobenzonitrile | HCID 14517 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Methylpyridine-2-ethanol | HCID 70283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[2-(6-Methyl-2-pyridyl)ethoxy]benzonitrile | HCID 14211279 | — |
Reaction Steps
To a mixture of 6-methyl-2-pyridineethanol (97.2 g), p-fluorobenzonitrile (85.8 g) and dry tetrahydrofuran (600 ml) was added 60% sodium hydride in oil (29.0 g) in small portions with ice-cooling and stirring and the mixture was further stirred for 2 hours. The reaction mixture was poured in ice-water and extracted with ethyl ether. The ethyl ether layer was washed with water, dried (MgSO4) and concentrated, and the residue was crystallized from hexane to give 4-[2-(6-methyl-2-pyridyl)ethoxy]benzonitrile. Yield: 85.9 g (50.1%); m.p.: 66°-67° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE036575 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-acf753d5931c41a088c9e9f901a015e2 |
| Source note | uspto-grants-2000_02 |