Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039566Generated: November 2, 2026

Formaldehyde → 1-Methylpiperidine-4-carboxamide

https://huagongshe.com/reaction/2039566

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 43 h. The catalyst was filtered off through Celite and the latter 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 numberUS08580782B2
Source datasetuspto-grants-2013_11
ORD IDord-1dd9d30b8dc9440c8428a65d8f51fcc7
Source noteuspto-grants-2013_11