Potassium Permanganate → 4,6-Dimethylpicolinic acid

HRID 273451Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 273451
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[N:5]=[C:4]([CH2:9][OH:10])[CH:3]=1.[Mn]([O-])(=O)(=O)=[O:12].[K+]>O>[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[N:5]=[C:4]([C:9]([OH:12])=[O:10])[CH:3]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
2.5 °C

Versuchsvorschrift

4,6-Dimethyl-2-pyridinemethanol (7.5 g, 29.2 mmol) was added to 100 mL of water and stirred at 0-5° C. A solution of 5.3 g (32.1 mmol) of potassium permanganate in 100 mL of water was added portion-wise over 30 min while maintaining the temperature at 5-10° C. This resulted in the formation of a black solid. The mixture was stirred at 5-10° C. for an additional 30 min and then allowed to stir at room temperature for 30 min. The mixture was filtered and the manganese dioxide washed with methanol. The methanol washings were combined with the water extracts and the solvent was removed. The resulting tan solid was redissolved in water and washed with chloroform. The water layer was separated and the water removed to yield 5.4 g of 4,6-dimethyl-2-pyridinecarboxylic acid. The product was characterized by HPLC/MS.

Aufarbeitung

  1. temperaturewhile maintaining the temperature at 5-10° C
  2. customThis resulted in the formation of a black solid
  3. stirringThe mixture was stirred at 5-10° C. for an additional 30 min
  4. stirringto stir at room temperature for 30 min
  5. filtrationThe mixture was filtered
  6. washthe manganese dioxide washed with methanol
  7. customthe solvent was removed
  8. dissolutionThe resulting tan solid was redissolved in water
  9. washwashed with chloroform
  10. customThe water layer was separated
  11. customthe water removed

Quellen und Nachweise

ORD-Eintrag
ord-31a9c249296b494db420ed91bbdd2ad1
Quelldatensatz
uspto-grants-2008_11
Patentnummer
US07456315B2

Notizen zur Reaktion

Wird geladen…