Benzoyl chloride, 3,4,5-trimethoxy- → HCID 53763441, Verbindung
Reaktionsgleichung
Cl.[NH2:2][C:3]1[CH:13]=[CH:12][C:6]([CH:7]=[CH:8][C:9]([OH:11])=[O:10])=[CH:5][CH:4]=1.[CH3:14][O:15][C:16]1[CH:17]=[C:18]([CH:22]=[C:23]([O:27][CH3:28])[C:24]=1[O:25][CH3:26])[C:19](Cl)=[O:20]>>[CH3:28][O:27][C:23]1[CH:22]=[C:18]([CH:17]=[C:16]([O:15][CH3:14])[C:24]=1[O:25][CH3:26])[C:19]([NH:2][C:3]1[CH:4]=[CH:5][C:6]([CH:7]=[CH:8][C:9]([OH:11])=[O:10])=[CH:12][CH:13]=1)=[O:20]Komponenten
3
Versuchsvorschrift
4-(3,4,5-Trimethoxybenzoylamino)-cinnamic acid was prepared as described in Example 3 from 5 g (0.0271 mol) of p-aminocinnamic acid hydrochloride and 3,4,5-trimethoxybenzoyl chloride.
Quellen und Nachweise
- ORD-Eintrag
- ord-9ee30ad3d4cb49a690d24ecd91f0e2db
- Quelldatensatz
- uspto-grants-1976_01
- Patentnummer
- US03931153