HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4-(1-Hydroxyethyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4'-Cyanoacetophenone | HCID 74044 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(1-Hydroxyethyl)benzonitrile | HCID 583335 | — |
Reaction Steps
4-Acetylbenzonitrile (3 g, 20.67 mmol) was dissolved in THF (5 mL) and MeOH (5 mL) and cooled to 0° C. NaBH4 (0.782 g, 20.67 mmol) was added slowly. The reaction aged at rt for 30 min and was concentrated. 2M aq HCl was added and the solution was extracted with EtOAc. The organic layer was washed with water, dried with Na2SO4, filtered and concentrated to provide the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08278304B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-44fe43f1ced14970afa942b80192800b |
| Source note | uspto-grants-2012_10 |