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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388408Generated: November 1, 2026

2-Methylimidazole → 4-[3-(2-methyl-1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehyde

https://huagongshe.com/reaction/1388408

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylimidazoleHCID 12749—
ReactantSodium hydrideHCID 24758—
Reactant4-(3-Bromopropyl)-1-piperidinecarboxaldehydeHCID 20239768—
SolventDimethylformamideHCID 6228—
Product4-[3-(2-methyl-1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehydeHCID 2023978288%

Reaction Steps

A mixture of 2-methylimidazole (2 g, 0.025 M) and sodium hydride (1.2 g, 50% in mineral oil, 0.025 M) in dimethylformamide (20 ml) was stirred at room temperature for 1/2 hr. The reaction mixture was then heated at 50° C. and the solution of 4(3-bromopropyl)piperidine carboxaldehyde (4.6 g, 0.02 M) in dimethylformamide (20 ml) was added slowly. After completing the addition, the reaction was heated at 50° C. for 4 hrs and then solvent was removed in vacuo. Water (80 ml) was added to the residue and the mixture was extracted with methylene chloride. The combined extracts, dried over sodium sulfate, were stripped to dryness to yield an oil. The oil was purified on silica gel column, eluted with methanol chloroform (1:9 v/v) to give 4-[3-(2-methyl-1H-imidazol-1-yl)-propyl]-1-piperidinecarboxaldehyde (3.86 g, 88% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04431653
Source datasetuspto-grants-1984_02
ORD IDord-2846eaa71cea4007a55a86030ff9be72
Source noteuspto-grants-1984_02