Reaktionsgleichung
[CH2:1]([O:3][C:4]([C:6]1[CH:11]=[CH:10][C:9]([NH:12][NH2:13])=[CH:8][CH:7]=1)=[O:5])[CH3:2].[CH3:14][N:15]=[C:16]=[S:17]>C1C=CC=CC=1>[CH2:1]([O:3][C:4]([C:6]1[CH:11]=[CH:10][C:9]([NH:12][NH:13][C:16]([NH:15][CH3:14])=[S:17])=[CH:8][CH:7]=1)=[O:5])[CH3:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In 100 ml of benzene were dissolved 9.3 g of 4-ethoxycarbonylphenylhydrazine and 3.6 g of methyl isothiocyanate and then the solution was refluxed with stirring. After heat-refluxing for 5 hours, the reaction mixture thus formed was cooled and crystals thus formed were collected by filtration to provide 1-(4-ethoxycarbonylphenyl)-4-methylthiosemicarbazide as colorless crystals. The product, 1-(4-ethoxycarbonylphenyl)-4-methylthiosemicarbazide thus obtained could be used for the subsequent reaction without being purified.
Aufarbeitung
- temperaturethe solution was refluxed
- temperatureAfter heat-refluxing for 5 hours
- customthe reaction mixture thus formed
- temperaturewas cooled
- customcrystals thus formed
- filtrationwere collected by filtration
Quellen und Nachweise
- ORD-Eintrag
- ord-5c53712d53eb40dc95edae7008cfcbf8
- Quelldatensatz
- uspto-grants-1987_06
- Patentnummer
- US04675276
Verknüpfte Notizen
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