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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132912Generated: October 25, 2026

Potassium Carbonate → 1-Boc-4-(2-chloro-6-nitrophenyl)piperazine

https://huagongshe.com/reaction/132912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-DichloronitrobenzeneHCID 18555—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventAcetonitrileHCID 6342—
Product1-Boc-4-(2-chloro-6-nitrophenyl)piperazineHCID 5876770470.2%

Reaction Steps

To a stirred solution of 1,2-dichloro-3-nitrobenzene (0.96 g, 5.0 mmol) and piperazine-1-carboxylic acid tert-butyl ester (0.93 g, 5.0 mmol) in acetonitrile (5 mL) was added of K2CO3 (1.38 g, 10 mmol). The mixture was heated at reflux for 48 h. The solvent was removed under reduced pressure. The crude material was partitoned between EtOAc (100 mL) and H2O (20 mL). The organic layer was washed with H2O (2×20 mL), dried over Na2SO4 and concentrated. Column chromatography (silica, 10-20% EtOAc/hexanes) provided 4-(2-chloro-6-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (1.2 g, 70%). TLC (silica, 20% EtOAc/hexanes): Rf=0.45. MS (electrospray): exact mass calculated for C15H20CIN3O4, 341.1; m/z found, 364.1 [M+Na]30 . 1H NMR (400 MHz, CDCl3) 7.56 (dd, J=8.2, 1.4 Hz, 1H), 7.50 (dd, J=8.2, 1.4 Hz, 1H), 7.13 (t, J=8.2 Hz, 1H), 3.38-3.56 (m, 4H), 3.06 (m, 4H), 1.48 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388011B2
Source datasetuspto-grants-2008_06
ORD IDord-684344737d874f748b52592cd98fb8a5
Source noteuspto-grants-2008_06