Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | Piperidine | HCID 8082 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 5-Chlorovaleronitrile | HCID 80474 | — |
| Edukt | Aluminium lithium hydride | HCID 21226445 | — |
| Edukt | HCID 86594854 | HCID 86594854 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 5-(Piperidin-1-yl)pentan-1-amine | HCID 7138447 | 59% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07910605B2 |
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| Quelldatensatz | uspto-grants-2011_03 |
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| ORD ID | ord-a848a1a768d44709b5ed7825f960b825 |
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| Quellennotiz | uspto-grants-2011_03 |
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