Phosphorus oxychloride → Ethyl 6-chloro-2-(2,4-difluorophenyl)pyridine-3-carboxylate

HRID 1257092Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1257092
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]1[C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:13][CH:12]=[CH:11][N+:10]=1[O-].P(Cl)(Cl)([Cl:23])=O>ClC(Cl)C>[Cl:23][C:11]1[CH:12]=[CH:13][C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[C:9]([C:3]2[CH:4]=[CH:5][C:6]([F:8])=[CH:7][C:2]=2[F:1])[N:10]=1

Komponenten

4

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 582235643-Pyridinecarboxylic acid, 2-(2,4-difluorophenyl)-, ethyl ester, 1-oxide2×

Produkt 1

HCID 21062879Ethyl 6-chloro-2-(2,4-difluorophenyl)pyridine-3-carboxylate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 63651,1-DichloroethaneLösungsmittel

Reaktionsbedingungen

Temperatur
72.5 °C

Versuchsvorschrift

To a nitrogen purged 500 mL, 3-necked flask, fitted with a reflux condenser, heating mantle and a thermocouple was charged 2-(2,4-difluorophenyl)-3-(ethoxycarbonyl)pyridine 1-oxide, 4 (21 g, 75 mmoles, 1.0 eq), followed by 150 mL dichloroethane. Phosphorous oxychloride (75 mL) was added in one aliquate with stirring, causing an immediate rise in temperature from 21 to 23° C. followed by gradual warming. The solution was heated under nitrogen to 70-75° C. (completeness of reaction determined by HPLC). The reaction was then cooled to room temperature and concentrated under vacuum to remove most of the POCl3. The remainder was quenched by slowly pouring onto 450 g of ice. The mixture (after the ice melted) was then extracted into methylene chloride (2×200 mL). The combined organics were dried (MgSO4), filtered through silica, eluted with methylene chloride, and concentrated to give the title Compound, 5, as an orange solid. 1H NMR (500.0 MHz, CDCl3) d 8.15 (d, J=8.2 Hz, 1H), 7.54 (td, J=8.5, 5.0 Hz, 1H), 7.34 (d, J=8.2 Hz, 1H), 6.96-6.92 (m, 1H), 6.79-6.74 (m, 1H), 4.16 (q, J=7.2 Hz, 2H), 1.10 (t, J=7.1 Hz, H) ppm.

Aufarbeitung

  1. customTo a nitrogen purged 500 mL, 3-necked flask
  2. customfitted with a reflux condenser
  3. temperatureheating mantle
  4. customfrom 21 to 23° C.
  5. custom(completeness of reaction determined by HPLC)
  6. temperatureThe reaction was then cooled to room temperature
  7. concentrationconcentrated under vacuum
  8. customto remove most of the POCl3
  9. customThe remainder was quenched
  10. additionby slowly pouring onto 450 g of ice
  11. extractionwas then extracted into methylene chloride (2×200 mL)
  12. dry with materialThe combined organics were dried (MgSO4)
  13. filtrationfiltered through silica
  14. washeluted with methylene chloride
  15. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-8e5f0261278d45dbb5c5807affb603bd
Quelldatensatz
uspto-grants-2013_06
Patentnummer
US08461345B2

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