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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376175Generated: October 25, 2026

Potassium Iodide → 5-(Piperidin-1-yl)pentan-1-amine

https://huagongshe.com/reaction/1376175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPiperidineHCID 8082—
ReactantPotassium CarbonateHCID 11430—
Reactant5-ChlorovaleronitrileHCID 80474—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 86594854HCID 86594854—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-(Piperidin-1-yl)pentan-1-amineHCID 713844759%

Reaction Steps

5-Chlorovaleronitrile (10 mmol), 20 mmol of piperidine, 20 mmol of potassium carbonate and a catalytic amount of potassium iodide in 50 ml of ethanol were refluxed for 6 hours. The solvent was removed under reduced pressure, the residue suspended in water and extracted with methylene chloride. The organic layer was purified by column chromatography on silica gel using methylene chloride/methanol/aqueous ammonia (90/10/1) as eluent (Yield: 59%). The product was added dropwise to a suspension of 25 mmol of lithium aluminium hydride in 25 ml of dry tetrahydrofurane at 0° C. After refluxing for 1 hour 10 ml of a saturated solution of sodium/potassium tartrate in water was added dropwise. The residue was filtered off and the filtrate purified by column chromatography on silica gel using methylene chloride/methanol/aqueous ammonia (90/10/1) as eluent. The residue was crystallized with hydrochloric acid from diethyl ether/2-propanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169928B2
Source datasetuspto-grants-2007_01
ORD IDord-598c19b4991f4225b133672250e3fcda
Source noteuspto-grants-2007_01