Sodium Hydroxide → HCID 9964564, Verbindung
Reaktionsgleichung
[OH:1][NH:2][C:3]([C:5]1[CH:6]=[C:7]([C:16]([O:18]CC)=[O:17])[CH:8]=[C:9]([C:11]([O:13]CC)=[O:12])[CH:10]=1)=[O:4].[OH-].[Na+]>CC(C)=O>[OH:1][NH:2][C:3]([C:5]1[CH:6]=[C:7]([C:16]([OH:18])=[O:17])[CH:8]=[C:9]([C:11]([OH:13])=[O:12])[CH:10]=1)=[O:4]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of diethyl 5-[(hydroxyamino)carbonyl]-1,3-benzenedicarboxylate (0.281 g, 1.0 mmol) in acetone (5 mL) was added 1.0 N NaOH (5 mL) at room temperature, and the mixture was stirred at room temperature for 2 hours. The solvent was removed under reduced pressure and the residue was taken up with 1 N HCl (15 mL) to give white precipitate. This material was dried under vacuum to give 0.096 g of white solid: 1H NMR (D2O) δ 8.52 (s, 2H), 8.76 (s, 1H). Elemental analysis calculated for CH7NO6.H2O: C, 44.45; H, 3.73; N, 5.76. Found: C, 44.47; H, 3.78; N, 5.74.
Aufarbeitung
- customThe solvent was removed under reduced pressure
- customto give white precipitate
- customThis material was dried under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-6b5af1f571734850ac299a2b6d32fafc
- Quelldatensatz
- uspto-grants-2007_05
- Patentnummer
- US07220780B2
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