Hydrochloric Acid → 4-(4-Chloro-2-nitrophenoxy)benzoic acid
Reaktionsgleichung
[Cl:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][C:7]2[CH:16]=[CH:15][C:10]([C:11]([O:13]C)=[O:12])=[CH:9][CH:8]=2)=[C:4]([N+:19]([O-:21])=[O:20])[CH:3]=1.[Li+].[OH-].Cl>CO>[Cl:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][C:7]2[CH:8]=[CH:9][C:10]([C:11]([OH:13])=[O:12])=[CH:15][CH:16]=2)=[C:4]([N+:19]([O-:21])=[O:20])[CH:3]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The compound from Example 34a (29.6 g, 96.2 mmol) in 200 mL of MeOH was treated with aqueous LiOH (1 M) and heated under reflux for 1 hour. Cooled to room temperature and acidified with aqueous HCl (1 M). Precipitate was filtered, washed with H2O and air-dried giving the title compound as a yellow solid (28.2 g, 100%).
Aufarbeitung
- temperatureheated
- temperatureunder reflux for 1 hour
- filtrationPrecipitate was filtered
- washwashed with H2O
- customair-dried
Quellen und Nachweise
- ORD-Eintrag
- ord-483264d12f1d475791adcace31aee041
- Quelldatensatz
- uspto-grants-2012_08
- Patentnummer
- US08236950B2
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