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 3 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 | US05958936 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-12a04a3e89584ad2a32e8de2018f6785 |
| Source note | uspto-grants-1999_09 |