Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462019Generated: October 31, 2026

Piperazine → 1-(2-Piperidin-1-yl-ethyl)-piperazine

https://huagongshe.com/reaction/1462019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantSodium CarbonateHCID 10340—
Reactant1-(2-Chloroethyl)piperidineHCID 74827—
Solvent1-PentanolHCID 6276—
Product1-(2-Piperidin-1-yl-ethyl)-piperazineHCID 2737212—

Reaction Steps

To a mixture of anhydrous piperazine, 10.0 grams, (0.116 moles) and sodium carbonate (12.3 grams, 0.116 moles) in 70 cc of 1-pentanol brought to the boiling point, is added slowly over a period of four hours, N-(2-chloroethyl)piperidine, (11.3 grams; 0.077 moles) diluted with 150 cc of 1-pentanol. After boiling for an additional period of four hours, the mixture is allowed to cool, it is then filtered and evaporated under reduced pressure. The oily residue is subjected to column chromatography using methanol and concentrated ammonium hydroxide in the ratio of 95:5. The desired product is obtained as an oil, but after standing for a few hours, it solidifies. Melting point is 60°-62° from diisopropyl ether. It forms a picrate: melting point 235°-237° C. (from ethanol); Rf=0.21, (MeOH-NH4OH 9.5:0.5); IR (nujol) max: 3240, 2780, 2760, 1445, 1325, 1300, 1140, 1125, 1105, 865, 770 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04457931
Source datasetuspto-grants-1984_07
ORD IDord-bab286f5fb2d4b49980486772ea1422a
Source noteuspto-grants-1984_07