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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919692Generated: October 25, 2026

Potassium Carbonate → 1-(3-Chloro-4-nitrophenyl)-4-methylpiperazine

https://huagongshe.com/reaction/1919692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-MethylpiperazineHCID 53167—
Reactant2-Chloro-4-fluoro-1-nitrobenzeneHCID 75017—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-(3-Chloro-4-nitrophenyl)-4-methylpiperazineHCID 23139607—

Reaction Steps

2-chloro-4-fluoronitrobenzene (1.0 eq, 1 g, 5.7 mmol), N-methyl piperazine (1.2 eq, 1.18 g, 6.84 mmol), potassium carbonate (2.0 eq, 1.6 g, 11.6 mmol) were stirred at 100° C. in DMF for 3 hours. The mixture was cooled down and diluted with water. The material was extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4 and the solvent evaporated in vacuo. After trituration in diethylether and filtration, 1-(3-chloro-4-nitrophenyl)-4-methylpiperazine was isolated as a solid (0.9 g, 62%). LCMS (ES): m/z 256 [M+1]+. This material was suspended in MeOH (20 ml) with Raney Nickel (0.2 g) and stirred under hydrogen atmosphere overnight. The catalyst was filtered off through celite. Evaporation of the solvents provided 2-chloro-4-(4-methylpiperazin-1-yl)aniline as a dark brown oil (0.68 g, 86%). LCMS (ES): m/z 226 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168651B2
Source datasetuspto-grants-2012_05
ORD IDord-147d905ba43d462ba6ab47f10fe2c133
Source noteuspto-grants-2012_05