HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(1-(Phenylmethyl)-4-piperidinyl)benzamide → N-4-Piperidylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(1-(Phenylmethyl)-4-piperidinyl)benzamide | HCID 40598 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-4-Piperidylbenzamide | HCID 118120 | 100% |
Reaction Steps
To a suspension of 10% palladium on carbon (0.2 g) in 30 mL of ethyl alcohol was added a solution of 1-benzyl-4-benzamido-piperidine (0.5 g, 1.79 mmol) in ethyl alcohol (10 mL). The resulting suspension was hydrogenated at 100 psi at 50° C. for 30 h after which it was filtered through a pad of celite and the solvent was removed in vacuo to obtain 0.34 g (100%) of 4-benzamidopiperidine as a white solid. It was used in the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06245773B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-2f29796371034863a69c1bad23542458 |
| Source note | uspto-grants-2001_06 |