HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → 4-amino-1-methylpiperidine-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | N-Methyl-2-piperidone | HCID 13603 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Product | 4-amino-1-methylpiperidine-4-carbonitrile | HCID 11434991 | — |
Reaction Steps
Using the procedure of Stage 1 of Example 1, 8 ml of ammonium hydroxide, 1.58 g of ammonium chloride and 1.23 g of sodium cyanide were reacted and 2.5 ml of 1-methylpiperidone were added. The mixture was stirred for 18 hours at ambient temperature, followed by extraction r3 times with chloroform. The organic phase was washed with salt water and dried to obtain 2.41 g of the expected product (orange-yellow syrup).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05646172 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-dc5971b1cb52476e8660ccef912bd5c0 |
| Source note | uspto-grants-1997_07 |