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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364725Generated: November 1, 2026

4[3-(1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehyde → 4-[3-(1H-imidazol-1-yl)propyl]piperidine

https://huagongshe.com/reaction/364725

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4[3-(1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehydeHCID 13726738—
Solvent1,4-DioxaneHCID 31275—
Product4-[3-(1H-imidazol-1-yl)propyl]piperidineHCID 1328119683.7%

Reaction Steps

A mixture of 4[3-(1H-imidazol-1-yl)propyl]-1-piperidinecarboxaldehyde (2.12 g, 0.0095M) in dioxane (80 ml) and 2NHCl (11 ml) was refluxed for 51/2 hrs. After the reaction, the solvent was removed, water was added and the solution was basified with 2N NaOH to pH 10 and extracted with CH2Cl2 (3×50 ml). The extracts were concentrated to give an oil (1.55 g, 80%). The dihydrochloride salt of the 4[3-(1H-imidazol-1-yl)propyl]-piperidine which was crystallized from acetone has m.p. 184°-186° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04605744
Source datasetuspto-grants-1986_08
ORD IDord-06ee1144acbf4cffa35693dc3f007df0
Source noteuspto-grants-1986_08