Methanol → Methyl pyridine-3-acetate

HRID 1475467

Reaktionsgleichung

Reaktionsgleichung von HRID 1475467
Cl.[N:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8][C:9]([OH:11])=[O:10])[CH:3]=1.S(Cl)(Cl)=O.[CH3:16]O>>[CH3:16][O:10][C:9](=[O:11])[CH2:8][C:4]1[CH:3]=[N:2][CH:7]=[CH:6][CH:5]=1

Komponenten

4

Versuchsvorschrift

A solution of pyridin-3-yl-acetic acid hydrochloride (10 g, 57.6 mmol) in MeOH (30 mL) was treated with thionyl chloride (4.2 mL, 57.6 mmol) and the mixture was stirred at room temperature for 2 h. Solvent was removed in vacuo and the residue was partitioned between saturated aqueous NaHCO3 and EtOAc. The organic phase was collected, dried over MgSO4 and evaporated to give the title compound (7.9 g) as a colourless oil. 1H NMR (CDCl3): 8.53 (2H, m), 7.64 (1H, d), 7.33-7.20 (1H, m), 3.72 (3H, s), 3.64 (2H, s).

Aufarbeitung

  1. customSolvent was removed in vacuo
  2. customthe residue was partitioned between saturated aqueous NaHCO3 and EtOAc
  3. customThe organic phase was collected
  4. dry with materialdried over MgSO4
  5. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-6c99a33576f245fca458856b513e8d9a
Quelldatensatz
uspto-grants-2015_04
Patentnummer
US09018214B2

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