2-Acetylpyridine → 3-Dimethylamino-1-(2-pyridyl)prop-2-en-1-one

HRID 2352187

Reaktionsgleichung

Reaktionsgleichung von HRID 2352187
[C:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][N:5]=1)(=[O:3])[CH3:2].CO[CH:12](OC)[N:13]([CH3:15])[CH3:14]>>[CH3:12][N:13]([CH3:15])[CH:14]=[CH:2][C:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][N:5]=1)=[O:3]

Komponenten

3

Edukt 2

HCID 142862-AcetylpyridineHCID 78373Dimethylformamide dimethyl acetal

Produkt 1

HCID 5669933-Dimethylamino-1-(2-pyridyl)prop-2-en-1-one

Versuchsvorschrift

A solution of 250 ml of 2-acetylpyridine and 500 ml of N,N-dimethylformamide dimethyl acetal was heated on a steam bath for 6 hours. After concentrating the reaction solution under vacuum, 1 liter of hexane was added to the part crystalline residue. The product was collected as small crystalline particles which were washed with an additional liter of hexane. Air drying was followed by drying at 45° C. under vacuum, leaving 350.7 g of 3-dimethylamino-1-(2-pyridinyl)-2-propen-1-one.

Aufarbeitung

  1. concentrationAfter concentrating the reaction solution under vacuum, 1 liter of hexane
  2. additionwas added to the part crystalline residue
  3. customThe product was collected as small crystalline particles which
  4. washwere washed with an additional liter of hexane
  5. customAir drying
  6. customby drying at 45° C. under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-960cfaa30cc64ec4a7b226743e3e7dc4
Quelldatensatz
uspto-grants-1989_10
Patentnummer
US04876252

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