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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541956Generated: November 1, 2026

Potassium Carbonate → tert-Butyl 4-(2-bromo-4-nitrophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/541956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-1-fluoro-4-nitrobenzeneHCID 69699—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-(2-bromo-4-nitrophenyl)piperazine-1-carboxylateHCID 5475874487%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 2-bromo-1-fluoro-4-nitrobenzene (0.1 g, 0.45 mmol) and tert-butyl piperazine-1-carboxylate (85 mg, 0.45 mmol) in N,N-dimethylformamide (0.9 mL) was treated with potassium carbonate (94 mg, 0.68 mmol) and stirred at 20° C. for 23 h and at 60° C. for 3.5 h. The reaction mixture was diluted with water (10 mL) and ethyl acetate (20 mL). The organic layer was separated, washed with water (10 mL) and brine (10 mL), dried over anhydrous sodium sulfate, filtered, and evaporated to give a yellow oil. This material was purified by flash column chromatography to give the desired product (0.15 g, 87%) as a yellow solid. LCMS for C15H20BrN3O4Na (M+Na)+: m/z=407.9, 410.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-af3052012ea1464fa30e41c4ef18a86f
Source noteuspto-grants-2014_10