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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605972Generated: October 27, 2026

p-Fluoronitrobenzene → 1-Tert-butyl-4-(4-nitrophenyl)piperazine

https://huagongshe.com/reaction/605972

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Tert-butylpiperazineHCID 3530572—
Solvent1,4-DioxaneHCID 31275—
ProductAmmoniaHCID 222—
Product1-Tert-butyl-4-(4-nitrophenyl)piperazineHCID 57444158118.5%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of 1-fluoro-4-nitro-benzene (314 mg, 2.23 mmol) and 4-tert-butyl-piperazine (1 g, 3.34 mmol) in dioxane (15 mL) is added K2CO3 (1.65 mg, 11.9 mmol) and the reaction is stirred at 130° C. overnight. The solvent is evaporated under vacuum and the residue is partitioned between ethyl acetate and water. The organic layer is washed with brine, dried over MgSO4, filtered and concentrated to give a crude compound. Purification by silica gel column chromatography eluting with DCM followed by 99:1 DCM:NH3 (7M in MeOH) affords the title compound (348 mg, 55.4%). LCMS: Rt 3.87 min (99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915256B2
Source datasetuspto-grants-2011_03
ORD IDord-577d6d26b4564c8a92062e309778b44a
Source noteuspto-grants-2011_03