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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989040Generated: October 30, 2026

Hydrochloric Acid → 4-Carbobenzoxy-1-(o-nitrophenyl)piperazine-2-carboxylic acid

https://huagongshe.com/reaction/989040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthylenediaminetetraacetic AcidHCID 6049—
ReactantTriethylamineHCID 8471—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantDisodiumHCID 141233—
Reactant4-((Benzyloxy)carbonyl)piperazine-2-carboxylic acidHCID 5058362—
CatalystCopper chelateHCID 472011—
SolventWaterHCID 962—
Product4-Carbobenzoxy-1-(o-nitrophenyl)piperazine-2-carboxylic acidHCID 12109643—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-carbobenzyloxypiperazine-2-carboxylic acid, copper chelate in 750 ml water was added ethylenediaminetetracetic acid, disodium salt, dihydrate (7.9 g, 21 mmol). The mixture was heated to 80° C. for 3 h. The reaction mixture was then cooled to rt and concentrated to dryness. The residue was dissolved in 100 ml DMSO. 2-Fluoronitrobenzene (4.9 g, 35 mmol) and triethyl amine (20 ml, 143 mmol) were added and the solution was heated to 60° C. for 16 h. The dark reaction mixture was cooled to rt. Concentrated HCl was added to bring the pH to 3. The solution was then diluted with 500 ml water and the aqueous layer was extracted with ethyl acetate. The combined organics were washed with water, dried over MgSO4 and concentrated to afford 4-carbobenzyloxy-1-(2-nitrophenyl) piperazine-2-carboxylic acid used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638934B2
Source datasetuspto-grants-2003_10
ORD IDord-262184368b9346598f686db5021b4c43
Source noteuspto-grants-2003_10