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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 459724Erstellt: 24. Oktober 2026

Formaldehyde → 1-Methylpiperidine-4-carboxamide

https://huagongshe.com/de/reaction/459724

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
Edukt4-PiperidinecarboxamideHCID 3772—
KatalysatorPalladiumHCID 23938—
LösungsmittelWaterHCID 962—
Produkt1-Methylpiperidine-4-carboxamideHCID 33901164,5%

Reaktionsschritte

Isonipecotamide (10 g, 78.0 mmoles) was dissolved in distilled water (100 mL) and 37% aqueous formaldehyde (7.6 mL, equivalent to 2.81 g HCHO, 93.6 mmoles) was added. Wet 10% Pd—C (8 spoon spatulas) was added under argon and the mixture was hydrogenated at 25° C. and 50 psi for 43 h. The catalyst was filtered off through Celite and the latter was washed with water and methanol. The combined filtrates were evaporated to dryness and the residue was chromatographed on a silica gel column (60×5 cm) using 8%–10%–20% (10% conc. ammonium hydroxide in methanol)-dichloromethane as the eluant to give 1-methylisonipecotamide (7.15 g, 64%): FABMS: m/z 143.1 (MH+); HRFABMS: m/z 143.1184 (MH+). Calcd. for C7H15N2O: m/z 143.1184; δH (d6-DMSO) 1.50/1.57 (4H, m, CH2), 1.76/1.94 (4H, m, CH2), 2.10 (3H, s, —NCH3), 2.72 (1H, m, CH) and 6.68/7.18 ppm (2H, m, CONH2); δC (d6-DMSO)CH3: 41.2; CH2: 28.5, 28.5, 54.9, 54.9; CH: 46.2; C: 176.7.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07196078B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-967c34a506014927805b854263b564a2
Quellennotizuspto-grants-2007_03