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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182252Generated: October 26, 2026

Ethyl Acetate → Tert-butyl 4-(4-cyanophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2182252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-FluorobenzonitrileHCID 14517—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium BicarbonateHCID 516892—
SolventAcetonitrileHCID 6342—
ProductTert-butyl 4-(4-cyanophenyl)piperazine-1-carboxylateHCID 279551223.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-fluorobenzonitrile (3.6 g) and N-tert-butyloxycarbonylpiperazine (5.58 g) in acetonitrile (60 mL) was heated at 80° C. for 72 hours. The reaction mixture was then cooled to room temperature and then treated with a mixture of sodium bicarbonate solution and ethyl acetate (300 mL, 1:1, v/v). The organic phase was separated and then evaporated. The residue was subjected to chromatography on silica gel eluting with a mixtures of heptane and ethyl acetate (from 3:7 to 1:1, v/v) to give the title compound (2 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897207B2
Source datasetuspto-grants-2005_05
ORD IDord-f4f68f795977483f93ab1318de38b4c5
Source noteuspto-grants-2005_05