Potassium bisulfate → (S)-tert-butyl 1-oxohexan-2-ylcarbamate
Reaktionsgleichung
[H-].[Al+3].[Li+].[H-].[H-].[H-].CON(C)[C:10](=[O:24])[C@@H:11]([NH:16][C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])[CH2:12][CH2:13][CH2:14][CH3:15].S([O-])(O)(=O)=O.[K+]>CCOCC.O>[C:20]([O:19][C:17]([NH:16][C@@H:11]([CH2:12][CH2:13][CH2:14][CH3:15])[CH:10]=[O:24])=[O:18])([CH3:23])([CH3:22])[CH3:21]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- -45 °C
Versuchsvorschrift
A mechanically stirred suspension of lithium aluminum hydride (5.00 g, 0.131 mol) in ether (250 mL) was cooled to -45° C. under nitrogen. A solution of the product from Step A (28.3 g, 0.103 mol) in ether (125 mL) was added, maintaining the temperature below -35° C. When the addition was complete, the reaction was warmed to 5° C., then recooled to -45° C. A solution of potassium hydrogen sulfate (27.3 g, 0.200 mol) in water was slowly added, maintaining the temperature below -5° C. After quenching, the reaction was stirred at room temperature for 1 h. The mixture was filtered through Celite, the ether evaporated, and the remainder partitioned between ethyl acetate and 2% potassium hydrogen sulfate. After washing with saturated brine, drying over magnesium sulfate and solvent removal, the title compound was obtained.
Aufarbeitung
- temperaturemaintaining the temperature below -35° C
- additionWhen the addition
- temperaturethe reaction was warmed to 5° C.
- customrecooled to -45° C
- temperaturemaintaining the temperature below -5° C
- customAfter quenching
- filtrationThe mixture was filtered through Celite
- customthe ether evaporated
- customthe remainder partitioned between ethyl acetate and 2% potassium hydrogen sulfate
- washAfter washing with saturated brine
- dry with materialdrying over magnesium sulfate and solvent removal
Quellen und Nachweise
- ORD-Eintrag
- ord-f46754c10b3e46b4b31154f6708d2f9f
- Quelldatensatz
- uspto-grants-2000_05
- Patentnummer
- US06060038
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