Trifluoroacetic anhydride → ethyl 2-[(E)-2-phenylethenyl]-1,3-oxazole-4-carboxylate

HRID 902830

Reaktionsgleichung

Reaktionsgleichung von HRID 902830
C(=O)([O-])O.[Na+].Br[CH2:7][C:8](=O)[C:9]([O:11][CH2:12][CH3:13])=[O:10].[C:15]([NH2:25])(=[O:24])[CH:16]=[CH:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.FC(F)(F)C(OC(=O)C(F)(F)F)=O>O1CCCC1.C(OCC)(=O)C>[C:18]1(/[CH:17]=[CH:16]/[C:15]2[O:24][CH:7]=[C:8]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[N:25]=2)[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1

Komponenten

7

Edukt 4

HCID 9845Trifluoroacetic anhydrideHCID 121352-Propenamide, 3-phenyl-HCID 66144Ethyl bromopyruvateHCID 516892Sodium Bicarbonate2×

Produkt 1

HCID 5708074ethyl 2-[(E)-2-phenylethenyl]-1,3-oxazole-4-carboxylate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8028TetrahydrofuranLösungsmittel2×HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

Synthesis was conducted in accordance with the report (J. Org. Chem., 1996, Vol. 61, p. 6496) by Panek et al. Sodium hydrogencarbonate (22.8 g) and ethyl bromopyruvate (10.5 ml) were added to a solution of cinnamamide (10.0 g) in tetrahydrofuran (250 ml) at room temperature, and the mixture was heated under reflux for 48 hours. The reaction mixture was allowed to cool to room temperature, filtered through Celite and then concentrated under reduced pressure to obtain residue. Trifluoroacetic anhydride (30 ml) was added to a solution of this residue in tetrahydrofuran (30 ml) at 0° C., and the mixture was gradually warmed to room temperature. After the mixture was stirred for 63 hours, a saturated aqueous solution (500 ml) of sodium hydrogencarbonate and ethyl acetate (150 ml) were added to the reaction mixture, and a water layer was separated. The water layer was extracted with ethyl acetate (150 ml). The organic layers were combined, washed with saturated aqueous solution of sodium chloride (150 ml), dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=5:1→3:1) to obtain the title compound (10.9 g).

Aufarbeitung

  1. customSynthesis
  2. temperaturethe mixture was heated
  3. temperatureunder reflux for 48 hours
  4. filtrationfiltered through Celite
  5. concentrationconcentrated under reduced pressure
  6. customto obtain residue
  7. temperaturethe mixture was gradually warmed to room temperature
  8. customa water layer was separated
  9. extractionThe water layer was extracted with ethyl acetate (150 ml)
  10. washwashed with saturated aqueous solution of sodium chloride (150 ml)
  11. dry with materialdried over anhydrous sodium sulfate
  12. concentrationconcentrated under reduced pressure
  13. customThe residue was purified by column chromatography on silica gel (hexane:ethyl acetate=5:1→3:1)

Quellen und Nachweise

ORD-Eintrag
ord-4fa44543375944b29fb299146e9773a8
Quelldatensatz
uspto-grants-2008_04
Patentnummer
US07365205B2

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