Hydrochloric Acid → 1-Propanol, 2-[(tetrahydro-2H-pyran-2-yl)oxy]-
Reaktionsgleichung
[H-].[Al+3].[Li+].[H-].[H-].[H-].[O:7]1[CH2:12][CH2:11][CH2:10][CH2:9][CH:8]1[O:13][CH:14]([CH3:19])[C:15](OC)=[O:16].Cl>CCOCC>[O:7]1[CH2:12][CH2:11][CH2:10][CH2:9][CH:8]1[O:13][CH:14]([CH3:19])[CH2:15][OH:16]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
25.0 g of lithium aluminum hydride was suspended in anhydrous ether, and 36.7 g of the compound (5a) was added thereto, followed by stirring for 1 hour at 0° C. and 2 hours at room temperature and neutralization by addition of aqueous HCl solution at 0° C. The reaction mixture was subjected to extraction with ether and reduced pressure-distillation (60° C./0.3 mmHg) to obtain 28.0 g of the product. (Yield: 90.2 %)
Aufarbeitung
- extractionThe reaction mixture was subjected to extraction with ether and reduced pressure-distillation (60° C./0.3 mmHg)
Quellen und Nachweise
- ORD-Eintrag
- ord-de6757c150474efaa75ad8bb4802a4a0
- Quelldatensatz
- uspto-grants-1993_10
- Patentnummer
- US05252251
Notizen zur Reaktion
Wird geladen…