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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-(2-Chloroethyl)piperidine | HCID 74827 | — |
| Solvent | 1-Pentanol | HCID 6276 | — |
| Product | 1-(2-Piperidin-1-yl-ethyl)-piperazine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04457931 |
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| Source dataset | uspto-grants-1984_07 |
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| ORD ID | ord-bab286f5fb2d4b49980486772ea1422a |
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| Source note | uspto-grants-1984_07 |
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