HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → HCID 68299265, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 86707842 | HCID 86707842 | — |
| Solvent | Ammonia | HCID 222 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68299265 | HCID 68299265 | — |
Reaction Steps
(1-Methoxy-piperidin-4-yl)-acetaldehyde (1.7 g, 10.8 mmol) was added dropwise to a mixture of KCN (910 mg, 14 mmol) and NH4Cl (795 mg, 15 mmol) in 10 ml of 33% aqueous ammonia and 10 ml of water at room temperature. After stirring at room temperature for 30 minutes, the reaction mixture was diluted with 20 ml of water and extracted with CH2Cl2 three times. The combined organic layers were dried over sodium sulfate, filtered and concentrated under vacuum. The crude product was purified by column chromatography on silica gel. Yield: 1.0 g of 2-amino-3-(1-methoxy-piperidin-4-yl)-propionitrile as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946453B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-3d8149ff9a194e2eacde905df51c756c |
| Source note | uspto-grants-2015_02 |