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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (4-Benzylpiperazin-1-yl)-(4-trifluoromethylphenyl)amine | HCID 23081308 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Piperazin-1-yl-(4-trifluoromethylphenyl)amine | HCID 23081312 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07262212B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-7078ba9038ca44ab904a8d1407c24d0d |
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| Source note | uspto-grants-2007_08 |
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