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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879025Generated: October 25, 2026

Piperazine → 1-(2-Fluoro-3-(trifluoromethyl)phenyl)piperazine

https://huagongshe.com/reaction/1879025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant3-Bromo-2-fluorobenzotrifluorideHCID 2736320—
ReactantPotassium tert-butoxideHCID 23665647—
Catalyst(+-)-1,1'-Binaphthyl-2,2'-diyl hydrogen phosphateHCID 99589—
SolventTolueneHCID 1140—
Product1-(2-Fluoro-3-(trifluoromethyl)phenyl)piperazineHCID 5744804154.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 3-bromo-2-fluorobenzotrifluoride (1.72 g, 7.1 mmol) in toluene (50 ml) under nitrogen, was added piperazine (0.89 g, 10.6 mmol), potassium tert-butoxide (0.95 g, 9.9 mmol), b is (dibenzylideneacetone)palladium(0) (0.19 g, 0.21 mmol) and (+/−)-1,1′-binaphthyl-2,2′-diyl hydrogen phosphate (0.13 g, 0.21 mmol). The resulting mixture was heated at 80° C. for 20 h. Filtration through a pad of celite and evaporation of the filtrate gave 2.1 g of crude product. The residue was purified by flash column chromatography (ethylacetate/methanol, 1:1) to give the title compound (0.96 g). MS m/z (rel. intensity, 70 eV) 248 (M+, 23), 207 (10), 206 (bp), 190 (17), 163 (8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314126B2
Source datasetuspto-grants-2012_11
ORD IDord-b117c6ee86134eaebcd7517eb992f59a
Source noteuspto-grants-2012_11