HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → 2-(Benzyloxy)-4-fluorobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,4-Difluorobenzonitrile | HCID 77545 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Benzyloxy)-4-fluorobenzonitrile | HCID 21069828 | 39.7% |
Reaction Steps
To 2.5 mL benzyl alcohol in 80 mL THF is added 1.87 g NaH. After one hour stirring at room temperature, 5.0 g of 2,4-Difluorobenzonitrile is added. After stirring one hour, the reaction is quenched with excess water and concentrated in vacuo. The residue is redissolved in ethyl acetate and washed with water, brine, dried over sodium sulfate, filtered and concentrated in vacuo. The product is recrystallizde in carbon tetrachloride to give 3.24 g (39.7%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07205313B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-85313e45bf884ff39abd94182019d2ff |
| Source note | uspto-grants-2007_04 |