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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925385Generated: October 28, 2026

1-Methylpiperazine → 1-(2-Fluoro-4-nitrophenyl)-4-methylpiperazine

https://huagongshe.com/reaction/1925385

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant1,2-Difluoro-4-nitrobenzeneHCID 123053—
Product1-(2-Fluoro-4-nitrophenyl)-4-methylpiperazineHCID 278305449.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

N-Methylpiperazine (30 mL, 27.1 g, 0.268 mol) was cooled in ice/water while adding 3,4-difluoronitrobenzene (2.0 g, 0.0126 mol) with stirring. The mixture was then heated at 100° C. overnight, evaporated to remove all excess N-methylpiperazine and the residue dissolved in 1M—hydrochloric acid (30 mL). After washing twice with 20 mL portions of DCM the solution was basified with 5 M—sodium hydroxide (10 mL). The product was extracted into DCM (twice with 20 mL), dried over sodium sulphate and evaporated giving 1.50 g yellow oil which solidified on standing

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178557B2
Source datasetuspto-grants-2012_05
ORD IDord-8b07e03ab33644f2af540666dffd68aa
Source noteuspto-grants-2012_05