Formaldehyde → 2-(1-Methylpiperidin-4-yl)acetic acid
Reaktionsgleichung
[NH:1]1[CH2:6][CH2:5][CH:4]([CH2:7][C:8]([OH:10])=[O:9])[CH2:3][CH2:2]1.[CH2:11]=O>O.[Pd]>[CH3:11][N:1]1[CH2:6][CH2:5][CH:4]([CH2:7][C:8]([OH:10])=[O:9])[CH2:3][CH2:2]1Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
4-Piperidinylacetic acid (4 grams) (28.0 mmoles) from Preparative Example 5A was dissolved in water (50 ml) and 37% formalin (2.72 ml) (33.6 mmoles) was added. The mixture was hydrogenated over 10% Pd-C at 55 psi at 25° C. for 68 hours. The catalyst was filtered off and washed with water. The combined filtrates were evaporated to dryness to give the title compound (MH+ 158).
Aufarbeitung
- filtrationThe catalyst was filtered off
- washwashed with water
- customThe combined filtrates were evaporated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-b8c4978785b145318b998ee872de2e2b
- Quelldatensatz
- uspto-grants-1997_09
- Patentnummer
- US05672611
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