Réaction #452422

ord-616f9badae8b46b989d6741c7c90ed55

Équation de réaction

CC(=O)CCCCl
5-chloro-2-pentanone
CNC.Cl
dimethylamine hydrochloride
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(=O)CCCN(C)C
desired product
CC(=O)CCCN(C)C
N,N-dimethyl-5-amino-2-pentanone

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureat reflux for 2 hours
  2. 2
    TempératureThe reaction mixture was then cooled to room temperature
  3. 3
    Autrepartitioned between water and dichloromethane
  4. 4
    AutreThe phases were separated
  5. 5
    Extractionthe aqueous phase again extracted with dichloromethane
  6. 6
    Séchagedried over sodium sulfate
  7. 7
    Concentrationconcentrated under reduced pressure
  8. 8
    Lavageeluting with dichloromethane containing 10% methanol and 1% ammonium hydroxide
  9. 9
    Concentrationconcentrated under reduced pressure

Mode opératoire

A mixture of 21.77 gm (180.5 mMol) 5-chloro-2-pentanone, 13.40 gm (164.3 mMol) dimethylamine hydrochloride and 50.0 gm (361.8 mMol) potassium carbonate in 150 mL acetonitrile was stirred at room temperature for 2 days and then at reflux for 2 hours. The reaction mixture was then cooled to room temperature and partitioned between water and dichloromethane. The phases were separated and the aqueous phase again extracted with dichloromethane. All organic phases were combined, dried over sodium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with dichloromethane containing 10% methanol and 1% ammonium hydroxide. Fractions shown to contain product were combined and concentrated under reduced pressure. The desired product was then isolated by distillation.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06126932uspto-grants-2000_10