Hydrochloric Acid → 6-Isobutyl-5-methyl-nicotinic acid hydrochloride
Reaktionsgleichung
C([O:3][C:4](=[O:16])[C:5]1[CH:10]=[C:9]([CH3:11])[C:8]([CH2:12][CH:13]([CH3:15])[CH3:14])=[N:7][CH:6]=1)C.[ClH:17]>>[ClH:17].[CH2:12]([C:8]1[C:9]([CH3:11])=[CH:10][C:5]([C:4]([OH:16])=[O:3])=[CH:6][N:7]=1)[CH:13]([CH3:15])[CH3:14]Komponenten
3
Versuchsvorschrift
A solution of 6-isobutyl-5-methyl-nicotinic acid ethyl ester (3.75 g, 16.95 mmol) in 12.5% aq. HCl (50 mL) is stirred at 65° C. for 24 h before the solvent is evaporated. The residue is dried under HV to give 6-isobutyl-5-methyl-nicotinic acid hydrochloride (3.55 g) as a white powder; LC-MS: tR=0.57 min, [M+1]+=194.25.
Aufarbeitung
- customis evaporated
- customThe residue is dried under HV
Quellen und Nachweise
- ORD-Eintrag
- ord-80d37490514e4003814634beacaa4c4e
- Quelldatensatz
- uspto-grants-2012_10
- Patentnummer
- US08288554B2
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