Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1496962Generated: October 25, 2026

1,3-Dinitrobenzene → Tert-butyl 4-(3-fluoro-4-nitrophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1496962

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DinitrobenzeneHCID 7452—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactanttert-Butyl 4-(5-Fluoro-2-nitrophenyl)piperazine-1-carboxylateHCID 22272537—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-(3-fluoro-4-nitrophenyl)piperazine-1-carboxylateHCID 66738172—

Reaction Conditions

Temperature50 °C

Reaction Steps

2,4-dinitrobenzene (1.2 g), N-Boc-piperazine (1.4 g) and potassium carbonate (1.2 g) were dissolved in dimethylformamide (5 mL) and stirred at 50° C. overnight. Then, the mixture was distilled under reduced pressure to remove dimethylformamide, added with water, and extracted with ethyl acetate. The thus obtained organic layer was washed with brine, and water was removed with sodium sulfate, and the solvent was removed by distillation under reduced pressure. The mixture was purified by column chromatography (silica gel) to obtain target compounds (Rf=0.3, hexane:ethyl acetate=2:1) and (tert-butyl-4-(5-fluoro-2-nitrophenyl)piperazin-1-carboxylate (Rf=0.6, hexane:ethyl acetate=2:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199944B2
Source datasetuspto-grants-2015_12
ORD IDord-33434855225a4960ab79bee64b09fab3
Source noteuspto-grants-2015_12