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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430547Generated: November 1, 2026

1-(3-Fluoro-5-nitrobenzyl)-4-methylpiperazine → 3-Fluoro-5-((4-methylpiperazin-1-yl)methyl)aniline

https://huagongshe.com/reaction/1430547

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Fluoro-5-nitrobenzyl)-4-methylpiperazineHCID 86713682—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-Fluoro-5-((4-methylpiperazin-1-yl)methyl)anilineHCID 86713683100%

Reaction Steps

A solution of 1-(3-fluoro-5-nitrobenzyl)-4-methylpiperazine (0.15 g, 0.592 mmol) in MeOH (5 mL) was treated with 10% Pd—C (dry) (0.063 g, 0.059 mmol) and hydrogenated (1 atm) for 3 h. The solids were removed via filtration, rinsed with MeOH and the filtrate concentrated to dryness to afford 3-fluoro-5-((4-methylpiperazin-1-yl)methyl)aniline (100% yield assumed). MS (ESI) m/z: 224.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940756B2
Source datasetuspto-grants-2015_01
ORD IDord-d62c38f3fadd4e2e8b66b4c960672857
Source noteuspto-grants-2015_01