Reaktion #157714

ord-b708586464974af298207568eeaf91d3

Reaktionsgleichung

CI
methyl iodide
CCOC(=O)c1ccc(Cl)c(O)n1
ethyl 5-chloro-6-hydroxypyridine-2-carboxylate
CCOC(=O)c1ccc(Cl)c(OC)n1
ethyl 5-chloro-6-methoxypyridine-2-carboxylate
Ausbeute 80.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
70°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe reaction solution was filtered through celite
  2. 2
    Sonstigethe solvent was evaporated under reduced pressure
  3. 3
    SonstigeThe residue was purified by silica gel column chromatography (hexane:ethyl acetate=30:1)
  4. 4
    Sonstigepurified again by silica gel column chromatography (hexane:ethyl acetate=20:1)

Vorschrift

Silver carbonate (142.4 g) and methyl iodide (25 mL) were added to a solution of ethyl 5-chloro-6-hydroxypyridine-2-carboxylate (26.0 g) in chloroform (500 mL), and the mixture was stirred at 70° C. for seven hours. The reaction solution was filtered through celite, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=30:1) and purified again by silica gel column chromatography (hexane:ethyl acetate=20:1) to give ethyl 5-chloro-6-methoxypyridine-2-carboxylate as a white solid (22.3 g, 80%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08822503B2uspto-grants-2014_09