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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856071Generated: October 30, 2026

HCID 23081427, compound → HCID 6623740, compound

https://huagongshe.com/reaction/856071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23081427HCID 23081427—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 6623740HCID 662374094%

Reaction Steps

A mixture of (1-benzylpiperidin-4-yl)-(4-trifluoromethoxyphenyl)amine (3.0 g, 8.3 mmol) prepared in Reference Example 129 and a catalytic amount of 10% palladium/carbon in ethanol (30 ml) was refluxed under an atmospheric pressure of hydrogen for 20 hours. The reaction mixture was filtered through Celite, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (methylene chloride/methanol=10/1) to afford piperidin-4-yl-(4-trifluoromethoxyphenyl)amine (2.02 g, yield 94%) as a colorless crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-f8bc61d24b384ee0be338469491ce01e
Source noteuspto-grants-2007_08