Reaktion #6523

ord-d0ca2bb5fa8e4a7e9c2ffd5aff410073

Reaktionsgleichung

CCO
ethanol
O=C(O)c1cccnc1O
2-hydroxynicotinic acid
ClP(Cl)(Cl)(Cl)Cl
phosphorus pentachloride
O=P(Cl)(Cl)Cl
phosphorus oxychloride
CCOC(=O)c1cccnc1Cl
ethyl 2-chloronicotinate
Ausbeute 60.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThis was then heated at 120° C. for 2 hours
  2. 2
    EinengenThe reaction mixture was then concentrated in vacuo until a red viscous mass
  3. 3
    Sonstigewas obtained
  4. 4
    TemperaturThe latter was cooled in an ice water bath
  5. 5
    TemperaturIt was then refluxed for 30 min.
  6. 6
    Temperaturcooled
  7. 7
    SonstigeMost of the excess ethanol was removed under vacuo
  8. 8
    workup.ADDITIONthe remaining mass was diluted with water (90 ml.)
  9. 9
    Extraktionextracted with 2×100 ml
  10. 10
    WaschenThe organic layer was washed with 2N NaOH solution
  11. 11
    SonstigeIt was dried
  12. 12
    Einengenconcentrated
  13. 13
    Sonstigeto give a pale yellow liquid which
  14. 14
    workup.DISTILLATIONwas purified by distillation under reduced pressure (20 mm. Hg, b.p. 140°-44° C.)

Vorschrift

To a mixture of 2-hydroxynicotinic acid (13.91 g., 0.1 mole) and phosphorus pentachloride (42 g., 0.2 mole) was added phosphorus oxychloride (25 ml., excess) and then stirred at room temperature for 30 minutes. This was then heated at 120° C. for 2 hours. The reaction mixture was then concentrated in vacuo until a red viscous mass was obtained. The latter was cooled in an ice water bath and 45 ml. absolute ethanol was added first slowly and then rapidly. It was then refluxed for 30 min. and cooled. Most of the excess ethanol was removed under vacuo and the remaining mass was diluted with water (90 ml.). The aqueous solution was neutralized with 10% sodium carbonate solution and then extracted with 2×100 ml. portions of dichloromethane. The organic layer was washed with 2N NaOH solution followed by water and brine. It was dried and then concentrated to give a pale yellow liquid which was purified by distillation under reduced pressure (20 mm. Hg, b.p. 140°-44° C.) to give ethyl 2-chloronicotinate in 60-65% yield. A fore-run at 80°-110° C. (5-10%) was discarded which consisted mainly of ethyl 2-ethoxynicotinate.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05248781uspto-grants-1993_09