Reaktionsgleichung
[Cl:1][C:2]1[CH:14]=[CH:13][C:5]([C:6]([CH:8]([CH3:12])[C:9]([OH:11])=[O:10])=[O:7])=[CH:4][CH:3]=1.[N+:15]([O-])([OH:17])=[O:16]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([CH:8]([CH3:12])[C:9]([OH:11])=[O:10])=[O:7])=[CH:13][C:14]=1[N+:15]([O-:17])=[O:16]Komponenten
3
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
To fuming nitric acid (150 ml) was added p-chlorobenzoylpropionic acid (20.0 g), slowly portionwise at 0° C. After the addition was completed the resulting mixture was stirred at 0° C. for 30 minutes and the resulting white solid was suction filtered and washed with water until the pH of the washing liquids was neutral, then dried to yield 3-(4-chloro-3-nitrobenzoyl)propionic add as a white solid (13.0 g).
Aufarbeitung
- customslowly portionwise at 0° C
- additionAfter the addition
- filtrationthe resulting white solid was suction filtered
- washwashed with water until the pH of the washing liquids
- customdried
- customto yield 3-(4-chloro-3-nitrobenzoyl)propionic
Quellen und Nachweise
- ORD-Eintrag
- ord-4c442c2d85c24feebbe8e0084018a86b
- Quelldatensatz
- uspto-grants-1998_03
- Patentnummer
- US05728715
Verknüpfte Notizen
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