Reaktionsgleichung
[C:1]([NH:10][NH2:11])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[Cl:12][C:13]([Cl:19])([Cl:18])[C:14](=[NH:17])OC>>[Cl:12][C:13]([Cl:19])([Cl:18])[C:14]([NH:11][NH:10][C:1](=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4])=[NH:17]Komponenten
3
Versuchsvorschrift
A mixture of 3.8 g (0.025 mole) salicoylhydrazine and 10 ml (14.3 g, 0.08 mole) methyl 2,2,2-trichloroacetimidate was stirred 16 hours at room temperature. The solid that formed was washed with petroleum ether and dried to give 7.5 g (100% Yield; mp 168°-169° C.). The structure was confirmed via infrared and elemental analysis.
Aufarbeitung
- customThe solid that formed
- washwas washed with petroleum ether
- customdried
- customto give 7.5 g (100% Yield; mp 168°-169° C.)
Quellen und Nachweise
- ORD-Eintrag
- ord-88e76842bc034e489c23448c2f0c5573
- Quelldatensatz
- uspto-grants-1981_08
- Patentnummer
- US04282169
Verknüpfte Notizen
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