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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32733Generated: October 26, 2026

Benzene, 1-bromo-4-(trifluoromethyl)- → Rac-3-methyl-4-(4-trifluoromethyl-phenyl)-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/32733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-bromo-4-(trifluoromethyl)-HCID 67872—
Reactant2-(Dicyclohexylphosphino)biphenylHCID 2734216—
Reactanttert-Butyl 3-methylpiperazine-1-carboxylateHCID 2756810—
SolventTolueneHCID 1140—
ProductRac-3-methyl-4-(4-trifluoromethyl-phenyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 5979364331%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 3-Methyl-piperazine-1-carboxylic acid tert-butyl ester (1.0 g, 5.3 mmol) and of 1-Bromo-4-trifluoromethyl-benzene (1.0 g, 4.4 mmol) in toluene (10 ml) were added sodium-tert butylate (0.6 g, 6.2 mmol), 2-(dicyclohexylphosphino)biphenyl (31 mg, 89 mmol), and tris(dibenzylideneacetone)dipalladium-chloroform complex (23 mg, 22 mmol). The reaction mixture was then stirred for 16 hours at 80° C. After allowing to cool to room temperature the reaction mixture was concentrated in vacuo and purified by column chromatography (SiO2, 70 g, heptane/ethyl acetate 0-30%) to give the title compound as a light brown solid (0.47 g, 31%). MS (m/e): 345.2 (M+H+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427612B2
Source datasetuspto-grants-2008_09
ORD IDord-b63d2302b0744154adfd0d2fd8b18108
Source noteuspto-grants-2008_09