HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-((2,6-Dimethylpiperidino)amino)-3-phenylpropionitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenylacetaldehyde | HCID 998 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 2,6-Dimethyl-1-piperidylamine | HCID 123482 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-((2,6-Dimethylpiperidino)amino)-3-phenylpropionitrile | HCID 19802041 | 126.5% |
Reaction Steps
7.4 g of sodium cyanide, dissolved in 40 ml of water, and 18.0 g of phenyl acetaldehyde, dissolved in 30 ml of methanol, are added dropwise with ice-cooling to a mixture of 12.8 g of 1-amino-2,6-dimethylpiperidine, 60 ml of water and 8.6 ml of concentrated hydrochloric acid. The reaction mixture is stirred at room temperature for 3 days and extracted with dichloromethane. The combined organic phases are washed with water of pH 4-5 containing acetic acid, dried and concentrated in a rotary evaporator. 32.5 g of 2-((2,6-dimethylpiperidino)amino)-3-phenylpropionitrile are obtained, which are reacted further without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05179206 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-b0ebf0c816a74375901406c2b462383c |
| Source note | uspto-grants-1993_01 |