Water → 6-Fluoropyridine-2-carboxylic acid

HRID 352180

Reaktionsgleichung

Reaktionsgleichung von HRID 352180
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[N:3]=1.[Mn]([O-])(=O)(=O)=[O:10].[K+].[OH2:15]>>[F:1][C:2]1[N:3]=[C:4]([C:8]([OH:10])=[O:15])[CH:5]=[CH:6][CH:7]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

To a heterogeneous solution of 2-fluoro-6-methyl-pyridine (9.65 g, 86.8 mmol) in water (400 mL) was added potassium permanganate (31.6 g, 200 mmol), and the reaction was heated to approximately 100° C. After 30 minutes, additional potassium permanganate (16.5 g, 104 mmol) was added, and the reaction heated at 100° C. overnight. The reaction was filtered through celite to remove manganese salts. The mother liquor was washed with ethyl ether (200 mL×3), neutralized to pH 7, and concentrated down to approximately 100 mL total volume. The aqueous solution was acidified to pH 2 with concentrated HCl and extracted with ethyl acetate, followed by 20% i-PrOH/CHCl3 (×3). The combined organic layers were dried over MgSO4 and concentrated. The solids were suspended in chloroform, sonicated, then filtered to remove remaining side products. The mother liquor was concentrated to give 5.47 g as a white crystalline solid, 45% yield. 1H NMR: consistent with structure. MS (ion spray) 140 (M−).

Aufarbeitung

  1. temperaturethe reaction heated at 100° C. overnight
  2. filtrationThe reaction was filtered through celite
  3. customto remove manganese salts
  4. washThe mother liquor was washed with ethyl ether (200 mL×3)
  5. concentrationconcentrated down to approximately 100 mL total volume
  6. extractionextracted with ethyl acetate
  7. dry with materialThe combined organic layers were dried over MgSO4
  8. concentrationconcentrated
  9. customsonicated
  10. filtrationfiltered
  11. customto remove
  12. concentrationThe mother liquor was concentrated
  13. customto give 5.47 g as a white crystalline solid, 45% yield

Quellen und Nachweise

ORD-Eintrag
ord-a5c68623ed1b4ed084d1a993ff6dadcf
Quelldatensatz
uspto-grants-2004_06
Patentnummer
US06743794B2

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