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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866053Generated: October 30, 2026

Water → 4-aminocarbonyl-N-(4-propoxyphenylmethyl)piperidine

https://huagongshe.com/reaction/866053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-PiperidinecarboxamideHCID 3772—
ReactantPotassium BicarbonateHCID 516893—
Reactant1-(Chloromethyl)-4-propoxybenzeneHCID 12249108—
SolventTolueneHCID 1140—
Product4-aminocarbonyl-N-(4-propoxyphenylmethyl)piperidineHCID 1904093279.1%

Reaction Steps

The method taught by R. A. Farr et al, J. Org. Chem. 1981, 46, 1212-1215, was used in the following two-step preparation. A vigorously stirred solution of 16.5 grams (0.129 mole) of 4-aminocarbonylpiperidine, 25.0 grams (0.135 mole) of 4-propoxyphenylmethyl chloride, and 19.4 grams (0.193 mole) of potassium bicarbonate in 200 mL of toluene was heated at reflux for 6.5 hours. The reaction mixture was then cooled, water was added, and the mixture was extracted with ethyl acetate. The extract was washed with two portions of an aqueous solution saturated with sodium chloride. The organic layer was dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to a solid residue, which was slurried in pentane and collected by filtration, yielding 28.2 grams of 4-aminocarbonyl-N-(4-propoxyphenylmethyl)piperidine, mp 142°-146° C. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05569664
Source datasetuspto-grants-1996_10
ORD IDord-0bdf3c4da8a24475917f7120ee4b3488
Source noteuspto-grants-1996_10