HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2,6-Diethyl-2,3,6-trimethylpiperidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 2,6-Diethyl-2,3,6-trimethylpiperidin-4-one | HCID 22182213 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,6-Diethyl-2,3,6-trimethylpiperidin-4-amine | HCID 22486019 | — |
Reaction Steps
197.3 g of 2,6-diethyl-2,3,6-trimethylpiperidin-4-one are dissolved in 1.5 liters of methanol which is saturated with ammonia. This solution is hydrogenated in a 3 liter-autoclave at a hydrogen pressure of 100 bar in the presence of 30 g of Raney nickel. After 24 hours, the solution is filtered and the solvent evaporated. The residue is distilled in vacuo yielding 162 g 2,6-diethyl-2,3,6-trimethyl-4-aminopiperidine (compound no. 1) distilling at 133°-35° C. at 23 mm Hg. Using a methanolic solution of methylamine, n-butylamine, n-hexylamine, n-dodecylamine, benzylamine and 2-amino-ethanol, respectively, instead of the ammonia solution while otherwise following the procedure described above, there are obtained:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04191683 |
| Source dataset | uspto-grants-1980_03 |
| ORD ID | ord-febe0f886c384ae7a33273452e9d3ab4 |
| Source note | uspto-grants-1980_03 |