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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389754Generated: October 27, 2026

4-Nitrobenzoic Acid → Tert-butyl 4-(4-nitrobenzoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/389754

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoic AcidHCID 6108—
Reactant4-MethylmorpholineHCID 7972—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(4-nitrobenzoyl)piperazine-1-carboxylateHCID 276445994%

Reaction Conditions

Temperature20 °C

Reaction Steps

4-Nitrobenzoic acid (1.00 g, 6.00 mmol), tert-butyl 1-piperazinecarboxylate (1.10 g, 6.00 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.70 g, 9.00 mmol) and N-methylmorpholine (1.30 ml, 12.00 mmol) were dissolved in dichloromethane (10 ml) and the reaction mixture stirred at 20° C. for 5 h. The reaction was then washed with saturated sodium bicarbonate solution and brine. The organic phase was dried over MgSO4 and the solvent removed in vacuo. The residue was purified by silica gel column chromatography using a 0-50% EtOAc in hexane gradient to afford tert-butyl 4-(4-nitrobenzoyl)piperazine-1-carboxylate (1.88 g, 5.60 mmol, 94%) as a white solid. LCMS (1) Rt: 2.01 min; m/z (ES+) No M+H+, but 280 (-tBu) and 236 (-Boc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378095B2
Source datasetuspto-grants-2013_02
ORD IDord-23665bbb3b3c4faf8db97b1776997eba
Source noteuspto-grants-2013_02