Reaktionsgleichung
[NH2:1][C:2]([NH2:4])=[S:3].[ClH:5].[CH3:6][C:7]1[C:13](=O)[CH:12]=[C:11]([CH3:15])[C:9](=[O:10])[CH:8]=1>C(O)C>[ClH:5].[NH2:1][C:2]1[S:3][C:12]2[C:11]([CH3:15])=[C:9]([OH:10])[CH:8]=[C:7]([CH3:6])[C:13]=2[N:4]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To 2.24 g of thiourea were added 60 ml of ethanol and 2.5 ml of concentrated hydrochloric acid, followed by stirring. Then a solution of 8.0 g of p-xyloquinone in ethanol (120 ml) was slowly added dropwise thereto. The reaction mixture was stirred at room temperature for 24 hours and then concentrated to about one-half. The crystals thus precipitated were separated by filtering and washed with a small amount of ethanol. Thus 6.80 g of the title compound was obtained in the form of white crystals.
Aufarbeitung
- stirringThe reaction mixture was stirred at room temperature for 24 hours
- concentrationconcentrated to about one-half
- customThe crystals thus precipitated
- customwere separated
- filtrationby filtering
- washwashed with a small amount of ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-0413705d505a4721ac07d69958786d93
- Quelldatensatz
- uspto-grants-1995_05
- Patentnummer
- US05420144
Verknüpfte Notizen
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