HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Potassium Cyanide → 1-Dimethylamino-4-hydroxy-piperidine-4-carbonitrile
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Potassium Cyanide | HCID 9032 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 1-(Dimethylamino)-4-piperidinone | HCID 56737782 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-Dimethylamino-4-hydroxy-piperidine-4-carbonitrile | HCID 86671308 | 67,2% |
Reaktionsschritte
A solution of 6.0 g 1-dimethylamino-piperidin-4-one (prepared as described in Journal of Medicinal & Pharmaceutical Chemistry, 4, 423-36; 1961) in 30 ml of dichloromethane is added to a mixture of 4.1 g potassium cyanide and 10.6 g sodium hydrogencarbonate in 30 ml of water. The resulting mixture is stirred at room temperature for 3 hours, then extracted with ethyl acetate, the organic layer dried over sodium sulfate, and the solvent evaporated. 4.8 g 1-Dimethylamino-4-hydroxy-piperidine-4-carbonitrile is obtained. 1H-NMR (CDCl3): 3.95 ppm (s, broad, 1H), 2.90 ppm (m, 2H), 2.68 ppm (m, 2H), 2.40 ppm (s, 6H), 2.15 ppm (m, 2H), 1.95 ppm (m, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08703165B2 |
| Quelldatensatz | uspto-grants-2014_04 |
| ORD ID | ord-61b3fabf40134bebaef07e460b75712f |
| Quellennotiz | uspto-grants-2014_04 |