Hydrochloric Acid → 6-(Hydroxymethyl)pyridine-3-carboxylic acid
Reaktionsgleichung
C[O:2][C:3](=[O:12])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][OH:11])=[N:6][CH:5]=1.Cl>[OH-].[Na+].CO>[OH:11][CH2:10][C:7]1[CH:8]=[CH:9][C:4]([C:3]([OH:12])=[O:2])=[CH:5][N:6]=1Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A solution of 6-hydroxymethyl-nicotinic acid methyl ester (0.400 g, 2.38 mmol) in 1.0 N NaOH (25.0 mL) and methanol (10.0 mL) was heated at 80° C. for 1 hour. The reaction mixture was cooled to room temperature and the pH was adjusted to 7.0 with 1.0 N HCl. The reaction mixture was concentrated in vacuo and the resulting salt was slurried in DMF and filtered to provide the title compound.
Aufarbeitung
- concentrationThe reaction mixture was concentrated in vacuo
- filtrationfiltered
Quellen und Nachweise
- ORD-Eintrag
- ord-59423fface8b427fb41c791457caea82
- Quelldatensatz
- uspto-grants-2010_03
- Patentnummer
- US07671043B2
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