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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856059Generated: October 27, 2026

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

https://huagongshe.com/reaction/856059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzene, 1-bromo-4-(trifluoromethyl)-HCID 67872—
Reactant4-Benzylpiperazin-1-amineHCID 12198453—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
CatalystBinap, (A+-)-HCID 634876—
SolventTolueneHCID 1140—
Product(4-Benzylpiperazin-1-yl)-(4-trifluoromethylphenyl)amineHCID 2308130859.8%

Reaction Steps

A mixture of 4-bromobenzotrifluoride (3.00 g, 13.3 mmol), 4-benzylpiperazin-1-yl-amine (3.06 g, 16.0 mmol), palladium acetate (60 mg, 0.267 mmol), (S)-(−)-BINAP (174 mg, 0.280 mmol) and sodium tert-butoxide (1.92 g, 20.0 mmol) in toluene (60 ml) was refluxed under a nitrogen atmosphere for 7 hours. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with brine, dried over sodium sulfate, and then filtered. The filtrate was concentrated under reduced pressure, and the residue was then purified by silica gel column chromatography (n-hexane/acetone=4/1) to afford (4-benzylpiperazin-1-yl)-(4-trifluoromethylphenyl)amine (2.666 g, yield 59%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-e7da10e85eaf4a6e8ae7eb290deae6b5
Source noteuspto-grants-2007_08