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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641787Generated: November 1, 2026

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

https://huagongshe.com/reaction/1641787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant2-Fluoro-5-nitrobenzonitrileHCID 519417—
SolventEthanolHCID 702—
Producttert-Butyl 4-(2-cyano-4-nitrophenyl)piperazine-1-carboxylateHCID 2222799559.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 2-fluoro-5-nitrobenzonitrile (500 mg, 3.0 mmol) in ethanol (35 mL) was treated with potassium carbonate (420 mg, 3.0 mmol) and piperazine-1-carboxylic acid tert-butyl ester (560 mg, 3.0 mmol). The reaction mixture was stirred at 80° C. for 1 h, then cooled and partitioned between ethyl acetate and water. The organic layer was then collected, dried over sodium sulfate, filtered and evaporated to a yellow residue. Purification using flash chromatography yielded 4-(2-cyano-4-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (590 mg, 59% yield) as a bright yellow solid. HRMS calcd for C16H20N4O4 (M+Na) 355.1377, obsd 355.1376.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08115011B2
Source datasetuspto-grants-2012_02
ORD IDord-f29d7ee986b546ebbdaea6eaf65c1150
Source noteuspto-grants-2012_02