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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353714Generated: October 25, 2026

1-(2-Fluoro-4-nitrophenyl)-4-methylpiperazine → 3-Fluoro-4-(4-methylpiperazin-1-yl)aniline

https://huagongshe.com/reaction/353714

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Fluoro-4-nitrophenyl)-4-methylpiperazineHCID 2783054—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product3-Fluoro-4-(4-methylpiperazin-1-yl)anilineHCID 278305593%

Reaction Steps

A solution of 1-(2-fluoro-4-nitrophenyl)-4-methylpiperazine (5.00 g, 20.9 mmol) (from Step A above) and 10% palladium-on-carbon (0.20 g, 0.2 mmol) in ethyl acetate (100 mL) and ethanol (50 mL) was hydrogenated at 50 psi in a Parr shaker for 4 h. The mixture was filtered through Celite™. The Celite™ was washed with ethyl acetate (50 mL) and the solvent was evaporated to give 3-fluoro-4-(4-methyl-1-piperazinyl)benzenamine as a white solid (4.05 g, 93%, mp 89-91° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756374B2
Source datasetuspto-grants-2004_06
ORD IDord-40ccea2273bd466c8a75b6bd9a65e458
Source noteuspto-grants-2004_06