Sodium Carbonate → 4-formylnaphthalene-1-carboxylic Acid
Reaktionsgleichung
[CH:1]([C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]([C:13]([O:15]C)=[O:14])=[CH:5][CH:4]=1)=[O:2].C([O-])([O-])=O.[Na+].[Na+]>O>[CH:1]([C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]([C:13]([OH:15])=[O:14])=[CH:5][CH:4]=1)=[O:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of the methyl 4-formylnaphthoate above (2.3 g, 1 mmol) and Na2CO3 (1.25 g, 12 mmol) in water (30 mL) was heated in a water bath for approximately 2 hr until a clear solution was obtained. The solution was cooled and filtered. The filtrate was acidified with conc. HCl to give a yellow precipitate. The solids were collected and dried over night to give the desired product (1.86 g, 87%).
Aufarbeitung
- temperaturewas heated in a water bath for approximately 2 hr until a clear solution
- customwas obtained
- temperatureThe solution was cooled
- filtrationfiltered
- customto give a yellow precipitate
- customThe solids were collected
- customdried over night
Quellen und Nachweise
- ORD-Eintrag
- ord-22c09f6d171b47e69b740c7145d15996
- Quelldatensatz
- uspto-grants-2003_09
- Patentnummer
- US06613942B1
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