Reaktionsgleichung
C([O:4][CH2:5][C:6]1[CH:11]=[CH:10][C:9]([CH2:12][O:13]C(=O)C)=[CH:8][N:7]=1)(=O)C.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[H-]>O1CCCC1>[OH:4][CH2:5][C:6]1[CH:11]=[CH:10][C:9]([CH2:12][OH:13])=[CH:8][N:7]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2,5-Di(acetoxymethyl)pyridine (0.05 mole) is reduced with lithium aluminum hydride (0.025 mole) in tetrahydrofuran (50 ml.) at 0° C. with stirring. After one hour, water is added to decompose excess hydride, and the mixture is concentrated to dryness. The residue is extracted with hot isopropanol (2 × 60 ml.) and the extract is concentrated to dryness to give 2,5-di(hydroxymethyl) pyridine.
Aufarbeitung
- concentrationthe mixture is concentrated to dryness
- extractionThe residue is extracted with hot isopropanol (2 × 60 ml.)
- concentrationthe extract is concentrated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-23a8c88d114e4af9a106bd89132db456
- Quelldatensatz
- uspto-grants-1977_12
- Patentnummer
- US04061759
Verknüpfte Notizen
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