HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343500Generated: October 26, 2026
Acetic Acid → 4-Phenylpiperidine-4-carboxamide monohydrochloride
https://huagongshe.com/reaction/343500
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (1-Benzyl-4-phenylpiperidine-4-carbonyl)-oxidoazanium | HCID 88146759 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Phenylpiperidine-4-carboxamide monohydrochloride | HCID 3017129 | — |
Reaction Steps
Combine 1-benzyl-4-phenylpiperidine-4-carboxylic acid amide N-oxide (529 g, 1700 mmol), 10% palladium-on-carbon (25 g), and acetic acid (5 L) in an autoclave. Flush the autoclave with nitrogen and then charge with 255 psi of hydrogen. Stir while recharging the autoclave with hydrogen as required to maintain the pressure above 100 psi. When hydrogen consumption ceases, flush the autoclave with nitrogen remove the catalyst by filtration. Evaporate the filtrate invacuo to give a residue. Dissolve the residue in ethyl acetate (5 L), acidify by the addition of 12M aqueous hydrochloric acid solution (150 mL), and heat to reflux for 15 minutes. Cool the mixture to 5° C. to give solid. Collect the solid by filtration, rinse with ethyl acetate, and air dry to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05861417 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-e08d54e5568f4fa695a5860fc3216475 |
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| Source note | uspto-grants-1999_01 |
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