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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270760Generated: October 30, 2026

Piperazine → 1-(4-(Trifluoromethoxy)phenyl)piperazine

https://huagongshe.com/reaction/270760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant1-Bromo-4-(trifluoromethoxy)benzeneHCID 521008—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
SolventTolueneHCID 1140—
Product1-(4-(Trifluoromethoxy)phenyl)piperazineHCID 23081170—

Reaction Conditions

Temperature110 °C

Reaction Steps

Piperazine (0.588 g, 6.84 mmol), Pd(II)acetate (0.027 g, 0.123 mmol), sodium t-butoxide (0.837 g, 10.06 mmol) and BINAP (0.154 g, 0.286 mmol) were stirred at room temperature in 10 mL dry toluene for 15 min. 4-trifluoromethoxy bromo benzene (1.5 g, 6.22 mmol) in 10 mL dry toluene was added into the reaction mixture. Then the reaction mixture was refluxed at 110° C. for 20 hrs. The reaction mixture was filtered through a celite bed, washed with toluene, concentrated, ethyl acetate added and then extracted with 1.5 (N) aqueous HCl solution three times. The combined aqueous layers were washed with diethyl ether. The aqueous layer was neutralized with 10% aqueous sodium hydroxide solution and then extracted with ethyl acetate three times. The combined ethyl acetate layers were washed with water and saturated brine solution, dried over anhydrous sodium sulfate and concentrated to afford the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449576B1
Source datasetuspto-grants-2008_11
ORD IDord-a9565e581aab4cce885c8be930e33743
Source noteuspto-grants-2008_11