Sodium hydride → 4-(3-Methoxypropoxy)-2,3-dimethyl-1-oxo-1lambda~5~-pyridine

HRID 727898Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 727898
[CH3:1][O:2][CH2:3][CH2:4][CH2:5][OH:6].[H-].[Na+].Cl[C:10]1[CH:15]=[CH:14][N+:13]([O-:16])=[C:12]([CH3:17])[C:11]=1[CH3:18]>CS(C)=O>[CH3:1][O:2][CH2:3][CH2:4][CH2:5][O:6][C:10]1[CH:15]=[CH:14][N+:13]([O-:16])=[C:12]([CH3:17])[C:11]=1[CH3:18]

Komponenten

5

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

2.0 g (22 mmol) of 3-methoxypropanol was dissolved in 50 ml of dimethyl sulfoxide to obtain a solution. 2.7 g (66 mmol) of sodium hydride was added to this solution at a room temperature. The obtained mixture was stirred at 60° C. for one hour and cooled to a room temperature by allowing to stand, followed by the addition of 3.0 g (19 mmol) of 4-chloro-2,3-dimethylpyridine N-oxide. The obtained mixture was stirred at 40° C. for one hour. After the completion of the reaction, the reaction mixture was distilled to remove the dimethyl sulfoxide. The obtained residue was purified by silica gel column chromatography to obtain 760 mg of 4-(3-methoxypropoxy)-2,3-dimethylpyridine N-oxide.

Aufarbeitung

  1. customto obtain a solution
  2. temperaturecooled to a room temperature
  3. stirringThe obtained mixture was stirred at 40° C. for one hour
  4. customAfter the completion of the reaction
  5. distillationthe reaction mixture was distilled
  6. customto remove the dimethyl sulfoxide
  7. customThe obtained residue was purified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-6065832ac4f342808f337ee295a7027f
Quelldatensatz
uspto-grants-1991_09
Patentnummer
US05045552

Notizen zur Reaktion

Wird geladen…