HuagongsheHuagongshe Chemistry Print Report · For research reference only
4'-Cyanoacetophenone → 4-(1-Hydroxyethyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4'-Cyanoacetophenone | HCID 74044 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(1-Hydroxyethyl)benzonitrile | HCID 583335 | 113.2% |
Reaction Steps
4-Acetylbenzonitrile (2.0 g; 13.8 mmol) was dissolved in THF (10 mL) and MeOH (10 mL). Sodium borohydride (782 mg; 20.7 mmol) was added portionwise at 0° C. and the reaction was let stirred at RT for 40 min. Solvents were removed under vacuum, EtOAC was added, and the organic phases were washed with H2O, dried over MgSO4, filtered and concentrated affording the title compound as a colorless oil (2.3 g, quantitative). HPLC (Method A) Rt 4.31 min (Purity: 99.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029405B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-4d6c6b7ef8ec498aa9bad1112e0ed9d5 |
| Source note | uspto-grants-2015_05 |