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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 604392Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/604392

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktPiperidineHCID 8082—
EduktPotassium CarbonateHCID 11430—
Edukt5-ChlorovaleronitrileHCID 80474—
EduktAluminium lithium hydrideHCID 21226445—
EduktHCID 86594854HCID 86594854—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-(Piperidin-1-yl)pentan-1-amineHCID 713844759%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07910605B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-a848a1a768d44709b5ed7825f960b825
Quellennotizuspto-grants-2011_03