Hydrogen Bromide → HCID 178510513, Verbindung
Reaktionsgleichung
Cl[C:2]1[N:9]=[CH:8][CH:7]=[C:6]([O:10]C)[C:3]=1[C:4]#[N:5].[BrH:12]>C(O)(=O)C>[Br:12][C:2]1[N:9]=[CH:8][CH:7]=[C:6]([OH:10])[C:3]=1[C:4]#[N:5]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 100 °C
Versuchsvorschrift
2-Chloro-4-methoxy-nicotinonitrile (M. Mittelbach et al., Arch. Pharm. (Weinheim Ger.); 1985, GE, 318, 6, 481-486) (6.92 g) was suspended in 70 mL of 30% HBr in acetic acid in a pressure vessel and heated with stirring at 100° C. for 2 h. The reaction was cooled to room temperature and filtered, washing well with H2O, and dried in vacuo overnight at 50° C. providing 4.85 g 2-bromo-4-hydroxy-nicotinonitrile as a white solid. Proton NMR(DMSO) indicated the product was a mixture of 69% bromo compound with 31% starting chloro analog.
Aufarbeitung
- temperatureheated
- temperatureThe reaction was cooled to room temperature
- filtrationfiltered
- washwashing well with H2O
- customdried in vacuo overnight at 50° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-3b15bcb75dcd474eb5d10ed895a53624
- Quelldatensatz
- uspto-grants-2005_11
- Patentnummer
- US06964956B2
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