Hydrogen Bromide → 4-Bromo-6-methylpyridine-2-carboxylic acid
Reaktionsgleichung
[CH3:1][C:2]1[N:7]=[C:6]([C:8]([OH:10])=[O:9])[CH:5]=[C:4]([N+]([O-])=O)[CH:3]=1.[BrH:14]>>[Br:14][C:4]1[CH:3]=[C:2]([CH3:1])[N:7]=[C:6]([C:8]([OH:10])=[O:9])[CH:5]=1Komponenten
3
Versuchsvorschrift
A solution of 3.6 g (19.6 mmol) of 6-Methyl-4-nitro-pyridine-2-carboxylic acid in 40 ml of 48% hydrobromic acid was heated at 100° C. overnight and then allowed to cool to room temperature. The solution was then evaporated to dryness in vaccuo. The crude material (10.5 g) containing inorganic salts was directly used in the next step.
Aufarbeitung
- customThe solution was then evaporated to dryness in vaccuo
- additionThe crude material (10.5 g) containing inorganic salts
Quellen und Nachweise
- ORD-Eintrag
- ord-7534d19fc07f4379a371d23045f25060
- Quelldatensatz
- uspto-grants-2011_05
- Patentnummer
- US07951824B2
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