HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzyl-4-piperidone → N~1~-(1-Benzylpiperidin-4-yl)-N~2~-phenylethane-1,2-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | 1,2-Ethanediamine, N1-phenyl- | HCID 74270 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N~1~-(1-Benzylpiperidin-4-yl)-N~2~-phenylethane-1,2-diamine | HCID 20540168 | — |
Reaction Steps
To the solution of 12.6 g of N-phenylethylenediamine in 200 ml of methanol, 50 ml of 4.1 N ethanolic hydrogen chloride are added dropwise followed by 18.9 g of 1-benzyl-4-piperidone in 100 ml of methanol. Then, 9.45 g sodium cyanoborohydride are added in portions while stirring at room temperature. After 72 hours the mixture is filtered, the residue dissolved in water and the solution made basic with 12.5% aqueous sodium hydroxide. It is extracted with methylene chloride, dried and evaporated to yield the 1-benzyl-4-(2-phenylaminoethylamino)-piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04073911 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-51fab4380d884453bbe2cd08d6aa7266 |
| Source note | uspto-grants-1978_02 |