2-Methyl-4-methoxypyridine-N-oxide → 4-Methoxy-2-methylpyridine

HRID 509437

Reaktionsgleichung

Reaktionsgleichung von HRID 509437
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][N+:6]([O-])=[C:5]([CH3:10])[CH:4]=1>CC(O)=O.[Fe]>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][N:6]=[C:5]([CH3:10])[CH:4]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

To a stirred solution of 4-methoxy-2-methylpyridine 1-oxide (20 g, 0.143 mol) in AcOH (200 mL, sdfine, India), was added Fe (16 g, 0.287 mol, sdfine, India) and the reaction mixture was stirred for 2 h at 120° C. The reaction mixture was concentrated and neutralized with sat'd NaHCO3. EtOAc was added to the mixture and it was filtered through Celite® brand filter agent. The organic layer was separated and the aqueous layer was extracted with EtOAc (3×150 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated to give the title compound as a brown liquid. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.33 (d, J=6 Hz, 1H), 6.68-6.64 (m, 2H), 3.84 (s, 3H), 2.52 (s, 3H). MS (ESI, positive ion) m/z: 124.0 (M+H).

Aufarbeitung

  1. concentrationThe reaction mixture was concentrated
  2. additionEtOAc was added to the mixture and it
  3. filtrationwas filtered through Celite® brand
  4. filtrationfilter agent
  5. customThe organic layer was separated
  6. extractionthe aqueous layer was extracted with EtOAc (3×150 mL)
  7. dry with materialThe combined organic layers were dried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-1fc9b8c7e57e4e74bcef376ed1d778ed
Quelldatensatz
uspto-grants-2015_08
Patentnummer
US09096527B2

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