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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1157381Erstellt: 26. Oktober 2026

Formaldehyde → 1-Methylpiperidine-4-carboxamide

https://huagongshe.com/reaction/1157381

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
PatentnummerUS07807683B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-05cdedd58d1f40989402cde78471bf93
Quellennotizuspto-grants-2010_10