HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sodium borohydride → (5-Bromo-2-(2-methylpiperidin-1-YL)phenyl)methanol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 5-Bromo-2-(2-methylpiperidin-1-YL)benzaldehyde | HCID 23091101 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Ammonium Chloride | HCID 25517 | — |
| Produkt | (5-Bromo-2-(2-methylpiperidin-1-YL)phenyl)methanol | HCID 58554197 | 97% |
Reaktionsschritte
To a solution of 5-bromo-2-(2-methylpiperidin-1-yl)benzaldehyde (16.30 g; 57.76 mmol) in MeOH (300 mL) was added sodium borohydride (2.19 g; 57.76 mmol) at 5° C. in a portion-wise fashion and stirred for 30 min. After this time, reaction mixture was diluted with a saturated aqueous solution of NH4Cl (300 mL), extracted with EtOAc. The org layers were washed with aqueous solution of NH4Cl (150 mL), brine (300 mL), dried over MgSO4 and evaporated under vacuum to give the title compound as a yellow oil (15.9 g, 97%). LC/MS (Method A): 285.6 (M+H)+. HPLC (Method A): Rt 2.13 min (Purity: 94.9%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08202865B2 |
| Quelldatensatz | uspto-grants-2012_06 |
| ORD ID | ord-7623db50dd62442a9174e143c5e24cd4 |
| Quellennotiz | uspto-grants-2012_06 |