Hydrochloric Acid → 6-Chloro-4-(trifluoromethyl)pyridine-2-carboxylic acid

HRID 19805Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 19805
Cl[C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[C:4]([CH3:12])[N:3]=1.[Mn]([O-])(=O)(=O)=[O:14].C([N+](CCCC)(CCCC)CCCC)CCC.OS([O-])=O.[Na+].[ClH:40].[OH2:41]>N1C=CC=CC=1>[Cl:40][C:2]1[N:3]=[C:4]([C:12]([OH:14])=[O:41])[CH:5]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:7]=1

Komponenten

7

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

To a solution of 300 mg of 2-chloro-6-methyl-4-(trifluoromethyl)-pyridine (1.49 mmol) in pyridine (5 ml) was added a solution of 1.61 g of tetrabutylammonium permanganate (4.46 mmol) in pyridine (4.5 ml) and the reaction mixture was stirred at 80° C. for 3 h. The reaction mixture was then poured into a mixture of water and ice and then NaHSO3 solution (40% in water) was added until the color turned light yellow. The mixture was then acidified by addition of 2N HCl and extracted with ethyl acetate. The combined organic layers were then washed with 1N HCl and brine, dried (Na2SO4), filtered and concentrated. The remaining residue was purified by chromatography (DCM/MeOH 100:0 to 90:10) to yield 224 mg (67%) of a gray liquid. MS (ISP) 224.3 (M−H)−.

Aufarbeitung

  1. extractionextracted with ethyl acetate
  2. washThe combined organic layers were then washed with 1N HCl and brine
  3. dry with materialdried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe remaining residue was purified by chromatography (DCM/MeOH 100:0 to 90:10)

Quellen und Nachweise

ORD-Eintrag
ord-ad385a6737f54efebaab70ef0ab45955
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07745477B2

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