Reaktionsgleichung
Cl[C:2]1[N:10]=[C:9]([Cl:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[NH3:12]>>[NH2:12][C:2]1[N:10]=[C:9]([Cl:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5]Komponenten
3
Reaktionsbedingungen
- Temperatur
- 135 °C
Versuchsvorschrift
A mixture of 2,6-dichloro-nicotinic acid (31 g, 0.14 mol) and 28% aqueous ammonia solution (200 mL) was stirred in a sealed tube for 10 hours at 135° C. This reaction solution was cooled to room temperature, and the excess ammonia gas was removed under a reduced pressure. Water was added to the residue to a total of 1000 mL, the mixture was cooled to 0° C., and citric acid was added to a pH being about 6. The precipitated solids were filtered out to obtain the title compound (12 g, 49%).
Aufarbeitung
- temperatureThis reaction solution was cooled to room temperature
- customthe excess ammonia gas was removed under a reduced pressure
- additionWater was added to the residue to a total of 1000 mL
- temperaturethe mixture was cooled to 0° C.
- additioncitric acid was added to a pH
- filtrationThe precipitated solids were filtered out
Quellen und Nachweise
- ORD-Eintrag
- ord-c6bcdac826aa4bd2aef409a03fd677ce
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08841327B2
Verknüpfte Notizen
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