HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → Phenylamino-1-(2-phenylethyl)-4-piperidinecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Phenylmethyl 4-(phenylamino)-1-(2-phenylethyl)-4-piperidinecarboxylate | HCID 12298150 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Phenylamino-1-(2-phenylethyl)-4-piperidinecarboxylic acid | HCID 86734310 | — |
Reaction Steps
A mixture of 60 parts of phenylmethyl 4-(phenylamino)-1-(2-phenylethyl)-4-piperidinecarboxylate and 320 parts of methanol is hydrogenated at normal pressure and at room temperature with 10 parts of palladium-on-charcoal catalyst 10%. Upon the addition of a concentrated ammonium hydroxide solution, the precipitate, which is formed during the hydrogenation, is dissolved. The catalyst is filtered off and the filtrate is concentrated. Methanol is added and the whole is concentrated again. After cooling to room temperature the product is filtered off and dried in vacuo at 120° C, yielding 43.7 parts of 4-(phenylamino-1-(2-phenylethyl)-4-piperidinecarboxylic acid; mp. 268° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03998834 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-c6692313b7da4e0aa778971ac01cf6cb |
| Source note | uspto-grants-1976_12 |