Ethanol → 1-Ethyl-3-carboxy-5,6-dimethyl-2-pyridone

HRID 1994252Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1994252
[CH2:1]([N:3]1[C:8]([CH3:9])=[C:7]([CH3:10])[CH:6]=C(C#N)[C:4]1=[O:13])[CH3:2].[OH-:14].[K+].[CH2:16]([OH:18])[CH3:17]>>[CH2:1]([N:3]1[C:8]([CH3:9])=[C:7]([CH3:10])[CH:6]=[C:17]([C:16]([OH:14])=[O:18])[C:4]1=[O:13])[CH3:2]

Komponenten

4

Reaktionsbedingungen

Temperatur
102 °C

Versuchsvorschrift

1-Ethyl-3-cyano-5,6-dimethyl-2-pyridone (3-003-03) (3.37 g) was dissolved in 80% ethanol (65 mL), and to the reaction mixture was added potassium hydroxide (7.96 g), and the reaction mixture was refluxed with stirring in oil bath at 102° C. for 24 h. The reaction mixture was evaporated under reduced pressure, and to the residue were added water (50 mL) and ethyl acetate (50 mL). After the reaction mixture was stirred under ice-cooling, and was separated by shaking, and to the aqueous layer was conc. hydrochloric acid (13 mL). The resulting crystal was filtered, and washed with cooled water to give 1-ethyl-3-carboxy-5,6-dimethyl-2-pyridone (3-003-04) (2.734 g, 73.3%, m.p. 164-165° C.) as a yellow ocher crystal.

Aufarbeitung

  1. temperaturethe reaction mixture was refluxed
  2. customThe reaction mixture was evaporated under reduced pressure
  3. additionto the residue were added water (50 mL) and ethyl acetate (50 mL)
  4. stirringAfter the reaction mixture was stirred under ice-
  5. temperaturecooling
  6. customwas separated
  7. stirringby shaking
  8. filtrationThe resulting crystal was filtered
  9. washwashed with cooled water

Quellen und Nachweise

ORD-Eintrag
ord-900c0038f3a6432a963082e1acda7587
Quelldatensatz
uspto-grants-2010_01
Patentnummer
US07652141B2

Notizen zur Reaktion

Wird geladen…