Acetic Acid → HCID 23051856, Verbindung
Reaktionsgleichung
[F:1][C:2]([F:15])([F:14])[C:3]1[CH:8]=[CH:7][C:6](/[CH:9]=[CH:10]/[C:11](=[O:13])[CH3:12])=[CH:5][CH:4]=1.[C:16]([OH:19])(=[O:18])[CH3:17]>O>[O:13]=[C:11](/[CH:10]=[CH:9]/[C:6]1[CH:5]=[CH:4][C:3]([C:2]([F:14])([F:15])[F:1])=[CH:8][CH:7]=1)/[CH:12]=[CH:17]/[C:16]([OH:19])=[O:18]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 12 g (56 mmol) of (E)-4-(4-trifluoromethylphenyl)but-3-en-2-one and 5.15 g (56 mmol) of glyoxlic acid monohydrate in 14 ml of acetic acid was heated at reflux for 20 hours. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic phase was extracted twice with 3N sodium hydroxide solution. The combined aqueous phases were treated with 3N hydrochloric acid to produce a strongly acidic reaction and extracted twice with ethyl acetate. The combined organic phases were dried over magnesium sulphate and concentrated. Crystallization of the residue from ether/hexane yielded (E,E)-4-oxo-6-(4-trifluoromethylphenyl)-2,5-hexadienoic acid of melting point 192°-195°.