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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10793Generated: October 26, 2026

Isobutyl iodide → 1-(Isobutyl)-4-(4-nitrophenyl)piperazine

https://huagongshe.com/reaction/10793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyl iodideHCID 10556—
ReactantPotassium CarbonateHCID 11430—
Reactant18-Crown-6HCID 28557—
Reactant1-(4-Nitrophenyl)piperazineHCID 80447—
SolventAcetonitrileHCID 6342—
Product1-(Isobutyl)-4-(4-nitrophenyl)piperazineHCID 21958910—

Reaction Steps

A mixture of 1-(4-nitrophenyl)piperazine (8 g, 38.6 mmol) (Acros Organics), powdered potassium carbonate (3.58 g, 25.98 mmol), 1-Iodo-2-methylpropane (4.66 ml, 40.5 mmol), and a catalytic amount of 18-crown-6 in acetonitrile (60 mL) was heated at reflux overnight. The mixture was filtered, and the filter cake was washed with acetonitrile. The solvent was evaporated from the combined filtrates and the residue was partitioned between water and ethyl acetate. The layers were separated and the aqueous layer was extracted twice with ethyl acetate. The combined organic layers were dried (Na2SO4), filtered, evaporated and dried under vacuum to give 1-(isobutyl)-4-(4-nitrophenyl)piperazine) (9.4 g, 92%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094896B2
Source datasetuspto-grants-2006_08
ORD IDord-4754a8151d09420396863f18deb623d8
Source noteuspto-grants-2006_08