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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
Reactant(1-Benzyl-4-phenylpiperidine-4-carbonyl)-oxidoazaniumHCID 88146759—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product4-Phenylpiperidine-4-carboxamide monohydrochlorideHCID 3017129—

Reaction Conditions

Temperature5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05861417
Source datasetuspto-grants-1999_01
ORD IDord-e08d54e5568f4fa695a5860fc3216475
Source noteuspto-grants-1999_01