Reaktionsgleichung
[CH2:1]([O:3][C:4]1[CH:11]=[CH:10][CH:9]=[CH:8][C:5]=1[CH:6]=O)[CH3:2].[CH2:12]([NH:16][OH:17])[CH2:13][CH2:14][CH3:15]>>[CH2:1]([O:3][C:4]1[CH:11]=[CH:10][CH:9]=[CH:8][C:5]=1[CH:6]=[N+:16]([CH2:12][CH2:13][CH2:14][CH3:15])[O-:17])[CH3:2]Komponenten
3
Versuchsvorschrift
The title compound was prepared according to the procedures described in Examples 11 using 2-ethoxybenzaldehyde and N-n-butylhydroxylamine. The title compound was isolated in 44.5% yield as a liquid.
Aufarbeitung
- customThe title compound was prepared
Quellen und Nachweise
- ORD-Eintrag
- ord-1cc4a1a0e91d4aed8493eb3c626f3912
- Quelldatensatz
- uspto-grants-2000_04
- Patentnummer
- US06046232
Verknüpfte Notizen
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