Reaktionsgleichung
[I-:1].[Na+].I.Cl[C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[CH:7][N:6]=1>CC(C)=O>[I:1][C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[CH:7][N:6]=1Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To 27.97 g (186.6 mmol) of sodium iodide cooled to -78° C. was added 121.77 g (71.6 ml, 952.0 mmol) of hydriodic acid (57 wt %). The reaction mixture was allowed to warm slightly with stirring for 5 minutes, and then 30.00 g (190.4 mmol) of 6-chloronicotinic acid was added. The resulting mixture was allowed to warm to room temperature with stirring and then heated at 120°-125° C. in an oil bath for 42 hours. A dark brown layer formed above the yellow solid material. The reaction mixture was allowed to cool to room temperature and then poured into acetone (chilled to 0° C.). The resultant yellow solid was collected by filtration, washed with 200 ml of 1N NaHSO3 solution, and dried in high vacuum (3 mm Hg) to give the title compound as a pale yellow solid.
Aufarbeitung
- temperatureto warm slightly
- stirringwith stirring
- temperatureheated at 120°-125° C. in an oil bath for 42 hours
- customA dark brown layer formed above the yellow solid material
- temperatureto cool to room temperature
- filtrationThe resultant yellow solid was collected by filtration
- washwashed with 200 ml of 1N NaHSO3 solution
- customdried in high vacuum (3 mm Hg)
Quellen und Nachweise
- ORD-Eintrag
- ord-b6665b274db740d495d2125d751f579c
- Quelldatensatz
- uspto-grants-1997_04
- Patentnummer
- US05618931
Verknüpfte Notizen
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