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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44639Generated: October 26, 2026

Triethylamine → 1-Tert-butyl-4-(4-nitrophenyl)piperazine

https://huagongshe.com/reaction/44639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactantp-FluoronitrobenzeneHCID 9590—
Reactant1-Tert-butylpiperazine dihydrobromideHCID 21906354—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product1-Tert-butyl-4-(4-nitrophenyl)piperazineHCID 57444158272.1%

Reaction Steps

A solution of 800 mg (5.67 mmol) of 1-fluoro-4-nitrobenzene, 2.07 g (1.2 mmol) of 1-tert-butylpiperazine dihydrobromide and 3.2 mL (20.41 mmol) of triethylamine, in 22 mL of acetonitrile, was refluxed for 10 hours. The mixture was cooled to room temperature, diluted with water and extracted with dichloromethane. The organic layer was washed with water and brine, dried over Na2SO4 and evaporated. Purification by flash chromatography (eluant dichloromethane/methanol 7/3) yielded 860 mg of the title compound as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541429B2
Source datasetuspto-grants-2013_09
ORD IDord-07072eefa89c499998446616e2b2cd7c
Source noteuspto-grants-2013_09