Potassium bisulfate → Tert-butyl N-(1-oxohex-4-YN-2-YL)carbamate

HRID 1956685Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1956685
[H-].[Al+3].[Li+].[H-].[H-].[H-].[C:7]([O:11][C:12]([NH:14][CH:15]([CH2:22][C:23]#[C:24][CH3:25])[C:16](N(OC)C)=[O:17])=[O:13])([CH3:10])([CH3:9])[CH3:8].S([O-])(O)(=O)=O.[K+]>CCOCC.O>[C:7]([O:11][C:12]([NH:14][CH:15]([CH2:22][C:23]#[C:24][CH3:25])[CH:16]=[O:17])=[O:13])([CH3:10])([CH3:9])[CH3:8]

Komponenten

6

Versuchsvorschrift

A suspension of lithium aluminum hydride (1.56 g, 41.1 mmol) in ether (150 mL) was stirred at room temperature for 30 minutes. The solution was cooled to -55° C. under nitrogen, and a solution of the product from Step J (11.10 g, 41.1 mmol) in ether (150 mL) was added over 15 min, maintaining the temperature below -50° C. When the addition was complete, the reaction was warmed to 5° C., then recooled to -40° C. A solution of potassium hydrogen sulfate (21.8 g) in 25 mL water was slowly added, maintaining the temperature below -35° C. The mixture was warmed to room temperature and stirred for one hour, filtered through Celite, and concentrated in vacuo to provide the title aldehyde.

Aufarbeitung

  1. temperatureThe solution was cooled to -55° C. under nitrogen
  2. temperaturemaintaining the temperature below -50° C
  3. additionWhen the addition
  4. temperaturethe reaction was warmed to 5° C.
  5. customrecooled to -40° C
  6. temperaturemaintaining the temperature below -35° C
  7. temperatureThe mixture was warmed to room temperature
  8. stirringstirred for one hour
  9. filtrationfiltered through Celite
  10. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-41bcdf6c8f63496e8b439867b782e0bb
Quelldatensatz
uspto-grants-1998_07
Patentnummer
US05780492

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