Reaktionsgleichung
[S:1]1[CH2:7][C:5](=[O:6])[NH:4][C:2]1=[S:3].[CH:8](=O)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.N1CCCCC1>C(O)C>[CH:8](=[C:7]1[S:1][C:2](=[S:3])[NH:4][C:5]1=[O:6])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 10 g (75.1 mmol) of rhodanine and 7.63 ml (75.1 mmol) of benzaldehyde in 150 ml of ethanol, 0.74 ml (7.5 mmol) of piperidine was added, and the mixture was heated under reflux for 5 hours. After cooling, the precipitated crystals were filtered and washed with cooled ethanol to give 1.07 g of the desired compound (66.6% yield, pale yellow crystals).
Aufarbeitung
- temperaturethe mixture was heated
- temperatureunder reflux for 5 hours
- temperatureAfter cooling
- filtrationthe precipitated crystals were filtered
- washwashed with cooled ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-4c6e2338edb642759fc7e265860d48de
- Quelldatensatz
- uspto-grants-1996_10
- Patentnummer
- US05561147
Verknüpfte Notizen
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