HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 12298154, compound → 4-Piperidinecarboxylic acid, 4-[(3-methoxyphenyl)amino]-, methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 12298154 | HCID 12298154 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Piperidinecarboxylic acid, 4-[(3-methoxyphenyl)amino]-, methyl ester | HCID 12298173 | — |
Reaction Steps
A mixture of 60 parts of methyl 4-[N-(3-methoxyphenyl)amino]-1-(phenylmethyl)-4-piperidinecarboxylate and 400 parts of ethanol is hydrogenated at normal pressure and at room temperature with 10 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen is taken up, the catalyst is filtered off and the filtrate is evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 10% of methanol, previously saturated with gaseous ammonia, as eluent. The pure fractions are collected and the eluent is evaporated, yielding methyl 4-[N-(3-methoxyphenyl)amino]-4-piperidinecarboxylate as an oily residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03998834 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-303ba88a098148aab14377f03007728a |
| Source note | uspto-grants-1976_12 |