Sodium Acetate → {2-[2-(4-Chloro-2-fluoro-phenyl)-vinyl]-oxazol-4-yl}-methanol
Reaktionsgleichung
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]=[CH:9][C:10]2[O:11][CH:12]=[C:13]([CH2:15]Cl)[N:14]=2)=[C:4]([F:17])[CH:3]=1.C([O-])(=[O:20])C.[Na+]>C(O)(=O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]=[CH:9][C:10]2[O:11][CH:12]=[C:13]([CH2:15][OH:20])[N:14]=2)=[C:4]([F:17])[CH:3]=1Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 2-[2-(4-chloro-2-fluoro-phenyl)-vinyl]-4-chloromethyl-oxazole (0.800 g, 2.94 mmol) and sodium acetate (0.482 g, 5.88 mmol) in acetic acid (10 ml) is refluxed for 55 h. The reaction mixture is cooled to r.t., concentrated in vacuo and the resulting residue is dissolved in ethanol (4 ml) and 5M potassium hydroxide (KOH) (15 ml). The solution is refluxed for 5 h and cooled to r.t. Saturated ammonium chloride (NH4Cl) is added and the mixture is extracted with ethyl acetate (3×). The extract is washed with brine, dried over Na2SO4 and concentrated in vacuo. The crude product is purified by flash column chromatography (ethyl acetate/hexanes 1:1) yielding {2-[2-(4-chloro-2-fluoro-phenyl)-vinyl]-oxazol-4-yl}-methanol as a colorless solid. Yield 0.582 g (78%).
Aufarbeitung
- concentrationconcentrated in vacuo
- dissolutionthe resulting residue is dissolved in ethanol (4 ml)
- temperatureThe solution is refluxed for 5 h
- temperaturecooled to r.t
- additionSaturated ammonium chloride (NH4Cl) is added
- extractionthe mixture is extracted with ethyl acetate (3×)
- washThe extract is washed with brine
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
- customThe crude product is purified by flash column chromatography (ethyl acetate/hexanes 1:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-7c352679c07549d7be4aa07fe8612a9a
- Quelldatensatz
- uspto-grants-2007_02
- Patentnummer
- US07179812B2
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