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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060988Generated: November 1, 2026

Sulfuric Acid → 1-[4-[(4-Fluorophenyl)methyl]phenyl]piperazine

https://huagongshe.com/reaction/1060988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPiperazineHCID 4837—
Reactant4,4'-DifluorobenzophenoneHCID 9582—
ReactantTriethylsilaneHCID 12052—
ReactantSodium HydroxideHCID 14798—
ReactantCarbonic acid, sodium saltHCID 24192197—
SolventAcetonitrileHCID 6342—
SolventTrifluoroacetic acidHCID 6422—
SolventTriethylamineHCID 8471—
Product1-[4-[(4-Fluorophenyl)methyl]phenyl]piperazineHCID 151999858%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a 10 ml acetonitrile solution of 426 mg of 4,4′-difluorobenzophenone and 841 mg of piperazine, 395 mg of triethylamine was added and stirred at 100° C. for 12 hours. After cooling to room temperature, saturated aqueous sodium hydrogenbicarbonate solution was added, followed by extracting with chloroform. The extract was dried, filtered and concentrated under reduced pressure. The residue obtained was dissolved in 5 ml of trifluoroacetic acid and treated with 520 mg of triethylsilane and 60 mg of concentrated sulfuric acid, and stirred at room temperature for 1 hour. The reaction, mixture was adjusted to pH=9 to 11 with 10% aqueous sodium hydroxide solution, followed by extracting with ethyl acetate. The extract was dried, filtered and concentrated under reduced pressure to give a residue, which was purified by silica gel column chromatography (chloroform:methanol:water (2% acetic acid)=65:35:5) to give the above-referenced compound, 1-[4-(4-fluorophenyl)methylphenyl]piperazine in an amount of 305 mg (yield 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525199B1
Source datasetuspto-grants-2003_02
ORD IDord-7cee15e3c0304fe88de934d351701f47
Source noteuspto-grants-2003_02