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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976146Generated: October 29, 2026

Ethanol → 4-[3-(1-Benzylpiperidin-4-yl)propanoyl]aniline

https://huagongshe.com/reaction/976146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant(E)-4-[3-(1-benzylpiperidin-4-yl)propenoyl]nitrobenzeneHCID 70279862—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventAcetic AcidHCID 176—
Product4-[3-(1-Benzylpiperidin-4-yl)propanoyl]anilineHCID 1996891937.5%

Reaction Steps

2.00 g of (E)-4-[3-(1-benzylpiperidin-4-yl)propenoyl]nitrobenzene was added to a mixed solvent of 30 ml of ethanol and 5 ml of acetic acid, and then 0.20 g of platinum oxide was added thereto. Thereafter, the mixture was stirred in a hydrogen stream at room temperature for 7.5 hours. After the reaction, the catalyst was removed by filtration, and the filtrate was condensed under reduced pressure. The obtained residue was applied to silica gel column chromatography to obtain 0.69 g of the title compound as pale yellow crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05610303
Source datasetuspto-grants-1997_03
ORD IDord-ae05ad79f9eb4e99b49d5b851aab7b27
Source noteuspto-grants-1997_03