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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856060Generated: October 30, 2026

(4-Benzylpiperazin-1-yl)-(4-trifluoromethylphenyl)amine → Piperazin-1-yl-(4-trifluoromethylphenyl)amine

https://huagongshe.com/reaction/856060

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Benzylpiperazin-1-yl)-(4-trifluoromethylphenyl)amineHCID 23081308—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductPiperazin-1-yl-(4-trifluoromethylphenyl)amineHCID 2308131290%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of (4-benzylpiperazin-1-yl)-(4-trifluoromethylphenyl)amine prepared in Reference Example 108 and 10% palladium/carbon (0.53 g) in ethanol (50 ml) was stirred at room temperature under an atmospheric pressure of hydrogen for 6 hours, and then at 60° C. for 10 hours. After the catalyst was removed by filtration through Celite, 10% palladium/carbon (0.53 g) was added to the filtrate, and the mixture was stirred at 60° C. under an atmospheric pressure of hydrogen for 8 hours. After the catalyst was removed by filtration through Celite, the filtrate was concentrated under reduced pressure. The resulting solid was dried in vacuo to afford piperazin-1-yl-(4-trifluoromethylphenyl)amine (1.76 g, yield 90%) as a colorless crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-7078ba9038ca44ab904a8d1407c24d0d
Source noteuspto-grants-2007_08