Methanol → Methyl 5-chloropyridine-2-carboxylate

HRID 1048355

Reaktionsgleichung

Reaktionsgleichung von HRID 1048355
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([OH:10])=[O:9])=[N:6][CH:7]=1.S(Cl)(Cl)=O.[CH3:15]O>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([O:10][CH3:15])=[O:9])=[N:6][CH:7]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

To a solution of 5-chloropyridin-2-carboxylic acid (309 g, 1.96 mol) in anhydrous MeOH (2 L) was slowly added thionyl chloride (299.7 mL, 4.12 mol, 2.1 eq) at room temperature (cloudy solution became clear brown solution during the addition of thionyl chloride). After the addition was complete, the reaction mixture was heated to 50° C. and stirred at this temperature overnight. The solvent and excess thionyl chloride were removed under reduced pressure and the crude product was azeotroped with toluene twice. The resulting solid was transferred to a filter funnel and washed with saturated aqueous NaHCO3 until the filtrate was basic. The resulting solid was dissolved in dichloromethane (2 L) and washed with saturated aqueous NaHCO3. The organics were dried over sodium sulfate, filtered and the filtrate was concentrated to provide the title compound as an off-white solid.

Aufarbeitung

  1. customat room temperature
  2. additionAfter the addition
  3. customThe solvent and excess thionyl chloride were removed under reduced pressure
  4. customthe crude product was azeotroped with toluene twice
  5. customThe resulting solid was transferred to a filter funnel
  6. washwashed with saturated aqueous NaHCO3 until the filtrate
  7. dissolutionThe resulting solid was dissolved in dichloromethane (2 L)
  8. washwashed with saturated aqueous NaHCO3
  9. dry with materialThe organics were dried over sodium sulfate
  10. filtrationfiltered
  11. concentrationthe filtrate was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-0fe30604df594b6e91f0bd2a2ec776e5
Quelldatensatz
uspto-grants-2013_10
Patentnummer
US08569341B2

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