Reaktion #11350

ord-46b5a06419784ab4aa0ab701d258a09a

Reaktionsgleichung

CCCC(=O)Cl
butyryl chloride
CCC(N)C(=O)O
2-aminobutyric acid
CCN(CC)CC
triethylamine
[Na+].[OH-]
sodium hydroxide
C[Si](C)(C)Cl
trimethylsilyl chloride
CCCC(=O)NC(CC)C(=O)O
2-Butyrylaminobutyric Acid

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturAfter cooling to −10° C.
  2. 2
    workup.STIRRINGthe resulting mixture is stirred at −10° C. for 2 hours and at room temperature for one hour
  3. 3
    TemperaturWith ice-cooling
  4. 4
    workup.STIRRINGthe reaction mixture is stirred at room temperature for 15 minutes
  5. 5
    Sonstigethe organic solvent is removed under reduced pressure
  6. 6
    Sonstigethe precipitated solid is triturated once with water and twice with petroleum ether
  7. 7
    Sonstigedried under reduced pressure at 45° C

Vorschrift

25.78 g of 2-aminobutyric acid (250 mmol) and 55.66 g (550 mmol) of triethylamine are dissolved in 250 ml of dichloromethane, and the solution is cooled to 0° C. 59.75 g (550 mmol) of trimethylsilyl chloride are added dropwise, and the solution is stirred at room temperature for 1 hour and at 40° C. for one hour. After cooling to −10° C., 26.64 g (250 mmol) of butyryl chloride are added dropwise, and the resulting mixture is stirred at −10° C. for 2 hours and at room temperature for one hour. With ice-cooling, 125 ml of water are added dropwise, and the reaction mixture is stirred at room temperature for 15 minutes. Aqueous sodium hydroxide solution is added to the organic phase, and the organic solvent is removed under reduced pressure. The residue is acidified and the precipitated solid is triturated once with water and twice with petroleum ether and dried under reduced pressure at 45° C. 29.1 g (67%) of a colorless solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07098207B2uspto-grants-2006_08