Reaktionsgleichung
[C:1](=[O:4])([O-])[O-].[Na+].[Na+].C(CS[C:12](=[S:18])SCC(O)=O)(O)=O.[C:19]([NH:27][NH:28][C:29]1[CH:34]=[CH:33][C:32]([NH2:35])=[CH:31][CH:30]=1)(=[O:26])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>O.C(O)C>[C:19]([NH:27][NH:28][C:29]1[CH:30]=[CH:31][C:32]([NH:35][C:12]([NH:35][C:32]2[CH:31]=[CH:30][C:29]([NH:28][NH:27][C:1](=[O:4])[C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)=[CH:34][CH:33]=2)=[S:18])=[CH:33][CH:34]=1)(=[O:26])[C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1Komponenten
6
Versuchsvorschrift
Sodium carbonate (4.65 g, 0.044 mole) was dissolved in a solvent mixture of water (95 ml) and ethanol (30 ml). Bis(carboxymethyl)trithiocarbonate (2.5 g, 0.011 mole) was added portionwise. Vigorous stirring of the reaction mixture was maintained until all solid was dissolved. It was then heated to 80°-85° C and 1-benzoyl-2-(4-aminophenyl)hydrazine (5.0 g, 0.022 mole) was added in one portion. Stirring and heating were maintained for one and one-half hour and the reaction mixture was then chilled. The solid was removed by filtration, washed and dried. Yield 2.05 g (37%), m.p. 185°-187° C.
Aufarbeitung
- temperaturewas maintained until all solid
- dissolutionwas dissolved
- temperatureIt was then heated to 80°-85° C
- stirringStirring
- temperatureheating
- temperaturewere maintained for one and one-half hour
- temperaturethe reaction mixture was then chilled
- customThe solid was removed by filtration
- washwashed
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-32d4633a0c2142058be403c8811ea4c0
- Quelldatensatz
- uspto-grants-1977_06
- Patentnummer
- US04030925
Verknüpfte Notizen
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