Sodium Hydroxide → HCID 9856593, Verbindung
Reaktionsgleichung
[CH3:1][C:2]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:9]2[NH:8][C:7](=[O:15])[C:6](=[O:16])[NH:5][C:4]=2[C:3]=1[C:17]([O:19]C)=[O:18].[OH-].[Na+]>C1COCC1>[CH3:1][C:2]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:9]2[NH:8][C:7](=[O:15])[C:6](=[O:16])[NH:5][C:4]=2[C:3]=1[C:17]([OH:19])=[O:18]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a suspension of 6-methyl-7-nitro-2,3-dioxo-1,2,3,4-tetrahydro-quinoxaline-5-carboxylic acid, methyl ester (0.80 g, 2.87 mmol) in THF (50 mL) was added aqueous 1.0N NaOH (4.3 mL, 4.3 mmol), and the reaction mixture was refluxed for 23 hours. The product is precipitated upon acidification with conc. HCL and recrystallized from water to give 0.73 g (96%).
Aufarbeitung
- temperaturethe reaction mixture was refluxed for 23 hours
- customThe product is precipitated upon acidification with conc. HCL
- customrecrystallized from water
- customto give 0.73 g (96%)
Quellen und Nachweise
- ORD-Eintrag
- ord-54e8e249a5524c0ca6c8a7aa9db7991b
- Quelldatensatz
- uspto-grants-2002_01
- Patentnummer
- US06340758B1
Notizen zur Reaktion
Wird geladen…