Reaktionsgleichung
Br[CH2:2][CH2:3][CH2:4][C:5](=[O:7])[CH3:6].[CH:8]1[C:21]2[C:20](=[C:22]3[CH2:27][CH2:26][NH:25][CH2:24][CH2:23]3)[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[O:13][C:12]=2[CH:11]=[CH:10][CH:9]=1.C(=O)([O-])[O-].[Na+].[Na+]>C(Cl)(Cl)Cl>[CH:18]1[C:19]2[C:20](=[C:22]3[CH2:27][CH2:26][N:25]([CH2:2][CH2:3][CH2:4][C:5](=[O:7])[CH3:6])[CH2:24][CH2:23]3)[C:21]3[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=3)[O:13][C:14]=2[CH:15]=[CH:16][CH:17]=1Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
7.2 g of 5-bromo-2-pentanone in 50 cc of chloroform are added dropwise to a suspension of 10.0 g of 4-(9-xanthenylidene)piperidine [M.P. 147°-149°, produced from N-methyl-4-(9-xanthenylidene)piperidine] and 9.25 g of sodium carbonate in 200 cc of chloroform. The reaction mixture is boiled at reflux for 17 hours, is filtered, concentrated by evaporation, the evaporation residue is placed on a column of 100 g of silica gel and elution is effected with chloroform containing 1% of methanol. The evaporation residue of the eluate is dissolved in acetone and made weakly acid to Congo red with hydrogen chloride in ether. The 5-[4-(9-xanthenylidene)piperidino]-2-pentanone hydrochloride which precipitates immediately is recrystallized from alcohol. M.P. 248°-251° (decomp.).
Aufarbeitung
- temperatureat reflux for 17 hours
- filtrationis filtered
- concentrationconcentrated by evaporation
- washthe evaporation residue is placed on a column of 100 g of silica gel and elution
- dissolutionThe evaporation residue of the eluate is dissolved in acetone
- customThe 5-[4-(9-xanthenylidene)piperidino]-2-pentanone hydrochloride which precipitates immediately
- customis recrystallized from alcohol
Quellen und Nachweise
- ORD-Eintrag
- ord-47ac54bf25334b349e0ffafc2ca17317
- Quelldatensatz
- uspto-grants-1978_02
- Patentnummer
- US04072756
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