HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345598Generated: October 30, 2026
HCID 15096799, compound → HCID 15096813, compound
https://huagongshe.com/reaction/345598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 15096799 | HCID 15096799 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15096813 | HCID 15096813 | — |
Reaction Steps
A solution of 22.9 parts of trans-N-[3-(phenylmethoxy)-1-(phenylmethyl)-4-piperidinyl]benzamide in 200 parts of methanol was hydrogenated at normal pressure and at room temperature with 3 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was suspended in 2,2'-oxybispropane. The product was filtered off and suspended in trichloromethane. The whole was shaken with a dilute ammonium hydroxide solution and the layers were separated. The aqueous phase was evaporated and the solid residue was suspended in 5 parts of water. The product was filtered off and dried, yielding 6 parts of trans-N-(3-hydroxy-4-piperidinyl)benzamide; mp. 210° C. (compound 218).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05057525 |
|---|
| Source dataset | uspto-grants-1991_10 |
|---|
| ORD ID | ord-371e327c78fc46da88c0671396306a37 |
|---|
| Source note | uspto-grants-1991_10 |
|---|