Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:4]=[C:5](N)[C:6](=[CH:10][CH:11]=1)[C:7]([OH:9])=[O:8].Cl.N([O-])=O.[Na+].[I-:18].[K+].OS(O)(=O)=O.II>O.C1(C)C=CC=CC=1>[I:18][C:5]1[CH:4]=[C:3]([O:2][CH3:1])[CH:11]=[CH:10][C:6]=1[C:7]([OH:9])=[O:8]Komponenten
Edukt 6
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 75 °C
Versuchsvorschrift
A mixture of 4-methoxyanthranilic acid (30.5 g, 0.18 mol), water (274.5 ml), and concentrated HCl (36.6 ml) was heated at 75° C. to effect solution and then was cooled to 0° C. The mixture was then treated with NaNO2 (13.3 g) in water (27.5 ml), followed by potassium iodide (45.75 g) in a water (75 ml)/H2SO4 (10.1 ml) solution. The reaction mixture was heated on a steam bath for 2 hours, then excess iodine was steam distilled. The reaction mixture was then cooled and the product was collected by filtration and dried in an oven at 75° C. To afford 39.28 g (78.6%) of crude product. The crude product was treated with toluene, the mixture was filtered and the filtrate was concentrated to afford 26.03 g of 2-iodo-4-methoxybenzoic acid.
Aufarbeitung
- temperaturewas cooled to 0° C
- temperatureThe reaction mixture was heated on a steam bath for 2 hours
- distillationdistilled
- temperatureThe reaction mixture was then cooled
- filtrationthe product was collected by filtration
- customdried in an oven at 75° C
- customTo afford 39.28 g (78.6%) of crude product
- filtrationthe mixture was filtered
- concentrationthe filtrate was concentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-593e53600721465ca80007ad82b445f8
- Quelldatensatz
- uspto-grants-1999_12
- Patentnummer
- US06008226
Verknüpfte Notizen
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