HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Phenyl-cyclohexanecarboxylic acid → (4-Phenylcyclohexyl)methanol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Phenyl-cyclohexanecarboxylic acid | HCID 344812 | — |
| Edukt | Aluminium lithium hydride | HCID 21226445 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (4-Phenylcyclohexyl)methanol | HCID 3100608 | 136% |
Reaktionsschritte
A suspension of LiAlH4 (0.56 g, 14.8 mmol, 2.0 equiv) was prepared under argon in 50 mL of anhydrous THF (50 mL) kept at 0° C. A solution of 4-phenyl-cyclohexanecarboxylic acid (1.5 g, 7.34 mmol, 1.0 equiv) in 50 mL of THF was added dropwise over a 20 min period. The reaction mixture was stirred at ambient temperature for 1.5 h and then cooled to 0° C. The excess hydride reagent was carefully quenched under argon by dropwise addition of 1 N HCl. After quenching, the reaction mixture was extracted with EtOAc. The organic layer was dried over MgSO4, filtered and concentrated to give the title product as a colorless oil (1.9 g crude) which was used without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06649642B2 |
| Quelldatensatz | uspto-grants-2003_11 |
| ORD ID | ord-56cd780c090840b79dbc6643f62ad871 |
| Quellennotiz | uspto-grants-2003_11 |