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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132928Generated: October 25, 2026

Potassium Carbonate → 4-(2,6-Dinitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/132928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Chloro-2,6-dinitrobenzeneHCID 11814—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventAcetonitrileHCID 6342—
Product4-(2,6-Dinitro-phenyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 8658481985%

Reaction Steps

To a stirred solution of 1.01 g (5.0 mmol) of 1-chloro-2,6-dinitrobenzene and 0.93 g (5.0 mmol) of 1-tert-butyloxycarbonylpiperazine in acetonitrile (5 mL) was added 1.38 g (10 mmol) of K2CO3. The mixture was heated to reflux for 48 h. The solvent was removed under reduced pressure. The crude product was partitioned between EtOAc (100 mL) and 20 mL of H2O. The organic layer was washed with H2O (2×20 mL), dried over Na2SO4 and concentrated. Column chromatography (silica, 10-20% EtOAc/hexanes) provided 1.31 g (85%) of 4-(2,6-dinitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester TLC (silica, 20% EtOAc/hexanes): Rf=0.35. 1H NMR (400 MHz, CDCl3): 7.75 (d, J=8.2 Hz, 2H), 7.25 (t, J=8.2 Hz, 1H), 3.30 (m, 4H), 2.95 (m, 2H), 1.44 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388011B2
Source datasetuspto-grants-2008_06
ORD IDord-1faa4d5c4f874f9da4e5f282eaafa8eb
Source noteuspto-grants-2008_06