HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 1-Benzyl-4-(cyanomethyl)piperidine-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Ethyl 2-(1-benzylpiperidin-4-ylidene)-2-cyanoacetate | HCID 424752 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Benzyl-4-(cyanomethyl)piperidine-4-carbonitrile | HCID 12847654 | 81.2% |
Reaction Steps
To a solution of (1-benzyl-piperidin-4-ylidene)-cyano-acetic acid ethyl ester (112.9 g, 0.40 mol) in EtOH (500 ml) and H2O (100 ml), potassium cyanide (64.6 g, 0.99 mol) is added at ambient temperature. The reaction mixture is stirred at 65 C.° for 24 h. After removal of EtOH, H2O is added to the residue. The waster phase is extracted with diethyl ether. The combined extracts are washed with H2O and brine, dried over sodium sulfate and evaporated down to give 77.7 g of 1-benzyl-4-cyanomethyl-piperidine-4-carbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531546B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-d14765825f544761824cd3df324f0815 |
| Source note | uspto-grants-2009_05 |