Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373435Generated: October 31, 2026

Formaldehyde → 1-Methylpiperidine-4-carboxamide

https://huagongshe.com/reaction/1373435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant4-PiperidinecarboxamideHCID 3772—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
Product1-Methylpiperidine-4-carboxamideHCID 33901164.5%

Reaction Steps

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 43h. 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07161003B1
Source datasetuspto-grants-2007_01
ORD IDord-fc89d117b0454d5683465edd8282a65c
Source noteuspto-grants-2007_01