Reaktion #523677
ord-ae2794e25b984ca29a251a1e2a2d4fdd
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturthe mixture was heated at its boiling point
- 2Temperaturunder reflux for 8 hours
- 3SonstigeThe solvent was then evaporated from the mixture under vacuum
- 4Sonstigethe residue was triturated with water
- 5Extraktionthe insoluble portion thereof was extracted
- 6workup.ADDITIONby the addition of a 5% aqueous sodium hydroxide solution
- 7Sonstigethe oily base which separated
- 8Extraktionwas extracted with ethyl ether
- 9TrocknenAfter drying the ether
- 10Extraktionextract over anhydrous sodium sulfate a solution of hydrogen chloride in ethanol
- 11workup.ADDITIONwas added
- 12Sonstigeprecipitated
- 13SonstigeThe crystals thus obtained
- 14Sonstigewere recrystallized in a mixture of ethanol and ethyl ether
- 15Sonstigewas obtained
Vorschrift
To a solution of 47.2 grams of 2-phenyl-3-acetyl benzofuran in 150 milliliters of isopropanol, were added 8.4 grams of paraformaldehyde, 30.8 grams of diethylamine hydrochloride and 3 milliliters of a saturated solution of hydrogen chloride in ethanol and the mixture was heated at its boiling point under reflux for 8 hours. The solvent was then evaporated from the mixture under vacuum and the residue was triturated with water and the insoluble portion thereof was extracted therefrom with ethyl ether. The aqueous solution was made alkaline by the addition of a 5% aqueous sodium hydroxide solution and the oily base which separated was extracted with ethyl ether. After drying the ether extract over anhydrous sodium sulfate a solution of hydrogen chloride in ethanol was added thereto and the crystalline hydrochloride of the compound named in the heading of this example precipitated. The crystals thus obtained were recrystallized in a mixture of ethanol and ethyl ether. In this manner, 34.2 grams of the recrystallized hydrochloride, which had a melting point of 113°-115°C, was obtained.