Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416654Generated: November 2, 2026

Water → Tert-butyl 3-methyl-4-(4-nitrophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2416654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl 3-methylpiperazine-1-carboxylateHCID 2756810—
SolventDimethyl SulfoxideHCID 679—
ProductTert-butyl 3-methyl-4-(4-nitrophenyl)piperazine-1-carboxylateHCID 22633044—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of (±)-tert-butyl 3-methylpiperazine-1-carboxylate (1.5 g), 1-fluoro-4-nitrobenzene (1.06 g) and potassium carbonate (2.07 g) in dimethyl sulfoxide (15 ml) was stirred at 120° C. for 15 hours. The reaction mixture was cooled to room temperature and poured into water (30 ml). The mixture was extracted with ethyl acetate three times. The combined organic layers were washed successively with water (twice) and brine, and dried over magnesium sulfate. The solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate 2:1) to give the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825200B1
Source datasetuspto-grants-2004_11
ORD IDord-ccc82224581841139373a20a59be8034
Source noteuspto-grants-2004_11