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

HRID 416569Notes

Reaction equation

HRID 416569 reaction equation
[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]

Participants

4

Conditions

Temperature
102 °C

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-03eb4b7b135a456eb933aa2a1644eb09
Source dataset
uspto-grants-2012_01
Patent number
US08088924B2

Reaction notes

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