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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892144Generated: November 2, 2026

tert-Butyl piperazine-1-carboxylate → 2-(3-Nitrophenyl)-1-(piperazin-1-yl)ethanone

https://huagongshe.com/reaction/1892144

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant3-Nitrobenzeneacetyl chlorideHCID 523225—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product2-(3-Nitrophenyl)-1-(piperazin-1-yl)ethanoneHCID 68728559—

Reaction Steps

2-(3-nitrophenyl)acetyl chloride (0.20 ml, 1.0 mmol.) was added to a vigorously stirred mixture of tert-butyl piperazine-1-carboxylate (0.19 g, 1.0 mmol.) in CH2Cl2 (2 ml) and sat. aq. NaHCO3 (1 ml). The reaction was stirred for 1 hour; then the organic layer was separated, filtered through a plug of MgSO4, and concentrated under vacuum. The residue was treated with TFA in CH2Cl2 to remove the Boc group to give 2-(3-nitrophenyl)-1-(piperazin-1-yl)ethanone, which was carried on crude.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507672B2
Source datasetuspto-grants-2013_08
ORD IDord-aeb5bc8838be4882a5e973d7c9da4429
Source noteuspto-grants-2013_08