Dimethylamine, hydrochloride → 5-(dimethylamino)pentan-2-one

HRID 843965Notes

Reaction equation

HRID 843965 reaction equation
Cl[CH2:2][CH2:3][CH2:4][C:5](=[O:7])[CH3:6].Cl.[CH3:9][NH:10][CH3:11].C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[CH3:9][N:10]([CH3:11])[CH2:2][CH2:3][CH2:4][C:5](=[O:7])[CH3:6]

Participants

5

Procedure

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.

Workup

  1. temperatureat reflux for 2 hours
  2. temperatureThe reaction mixture was then cooled to room temperature
  3. custompartitioned between water and dichloromethane
  4. customThe phases were separated
  5. extractionthe aqueous phase again extracted with dichloromethane
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated under reduced pressure
  8. washeluting with dichloromethane containing 10% methanol and 1% ammonium hydroxide
  9. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-1846ba87cfd545cdaa98f1a07ab3f58d
Source dataset
uspto-grants-2002_04
Patent number
US06380201B1

Reaction notes

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