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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917090Generated: November 1, 2026

Piperazine → 1-((2-(Trifluoromethyl)phenyl)methyl)piperazine

https://huagongshe.com/reaction/1917090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantTriethylamineHCID 8471—
Reactant1-(Bromomethyl)-2-(trifluoromethyl)benzeneHCID 123057—
SolventTolueneHCID 1140—
Product1-((2-(Trifluoromethyl)phenyl)methyl)piperazineHCID 302332268.2%

Reaction Steps

1.08 g (12.5 mmol) of piperazine are placed in the presence of 1 g (4.2 mmol) of 1-bromomethyl-2-trifluoromethyl-benzene and 0.64 mL (4.6 mmol) of triethylamine in 10 mL of toluene. The reaction medium is stirred for 30 min at room temperature and then heated to 110° C. for 6 h. After dry concentration, the obtained residue is taken up with AcOEt and washed with water. After drying on MgSO4, the organic phases are dry concentrated, the obtained residue is purified by flash chromatography on silica (CH2Cl2-MeOH—NH4OH: 90-9-1). 0.7 g of intermediate 7a are thereby isolated as a clear oil (yield 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618287B2
Source datasetuspto-grants-2013_12
ORD IDord-4836326672db4340a251e84a74df417a
Source noteuspto-grants-2013_12