Lithium Hydroxide → 5-Methoxyquinoline-3-carboxylic acid
Reaktionsgleichung
[CH2:1]([O:8][C:9]1[CH:18]=[CH:17][CH:16]=[C:15]2[C:10]=1[CH:11]=[C:12]([C:19]([O:21]CC)=[O:20])[CH:13]=[N:14]2)C1C=CC=CC=1.[Li+].[OH-]>C1COCC1.O>[CH3:1][O:8][C:9]1[CH:18]=[CH:17][CH:16]=[C:15]2[C:10]=1[CH:11]=[C:12]([C:19]([OH:21])=[O:20])[CH:13]=[N:14]2Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A solution of ethyl 5-methoxyquinoline-3-carboxylate (2.31 g, 10 mmol) prepared in stage B of example 2 and LiOH (0.4 g, 20 mmol) in THF (20 mL) and water (0.5 mL) was refluxed for 2 hours. After cooling, the solvents were evaporated under vacuum. The solid residue was used in the next step without further purification.
Aufarbeitung
- temperatureAfter cooling
- customthe solvents were evaporated under vacuum
- customThe solid residue was used in the next step without further purification
Quellen und Nachweise
- ORD-Eintrag
- ord-28339260fa2744bba8e1de1f258a4b27
- Quelldatensatz
- uspto-grants-2011_07
- Patentnummer
- US07977354B2
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