HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-((2,6-Dimethylpiperidino)amino)-3-methylbutyronitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isobutyraldehyde | HCID 6561 | — |
| 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-methylbutyronitrile | HCID 19802039 | — |
Reaction Steps
A solution of 4.9 g of sodium cyanide in 10 ml of water and a solution of 7.2 g of isobutyraldehyde in 30 ml of methanol are added dropwise with ice-cooling to a mixture of 6.4 g of 1-amino-2,6-dimethylpiperidine, 60 ml of water and 8.6 ml of concentrated hydrochloric acid. After stirring at room temperature for 8 days, the methanol is stripped off on a rotary evaporator and the solution is extracted with dichloromethane. The combined organic phases are washed with water of pH 5 containing acetic acid, dried and concentrated. 11.2 g of 2-((2,6-dimethylpiperidino)amino)-3-methylbutyronitrile remain, which are employed in the following step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05179206 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-c5b16b305d424d8f8eb99c380a0cb11b |
| Source note | uspto-grants-1993_01 |