Reaktionsgleichung
[C:1]([C:5]1[CH:6]=[C:7]([CH:10]=[C:11]([C:14]([CH3:17])([CH3:16])[CH3:15])[C:12]=1[OH:13])[CH:8]=O)([CH3:4])([CH3:3])[CH3:2].[CH3:18][N:19]([CH3:27])[N:20]1[C:24](=[O:25])[CH2:23][S:22][C:21]1=[S:26]>>[CH3:4][C:1]([C:5]1[CH:6]=[C:7]([CH:8]=[C:23]2[S:22][C:21](=[S:26])[N:20]([N:19]([CH3:27])[CH3:18])[C:24]2=[O:25])[CH:10]=[C:11]([C:14]([CH3:17])([CH3:16])[CH3:15])[C:12]=1[OH:13])([CH3:2])[CH3:3]Komponenten
3
Versuchsvorschrift
The title compound was prepared in 65% yield from 3,5-di-tert-butyl-4-hydroxybenzaldehyde and N-dimethylaminorhodanine following the procedure of Example 1.
Quellen und Nachweise
- ORD-Eintrag
- ord-ba95acd02ec1431cbddc769eeb52bb66
- Quelldatensatz
- uspto-grants-1993_06
- Patentnummer
- US05216002
Verknüpfte Notizen
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