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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558993Generated: October 29, 2026

1-(2-fluoro-4-nitrophenyl)-1H-pyrazole → [3-fluoro-4-(1H-pyrazol-1-yl)phenyl]amine

https://huagongshe.com/reaction/558993

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-fluoro-4-nitrophenyl)-1H-pyrazoleHCID 10703514—
CatalystMethanolHCID 887—
CatalystPalladiumHCID 23938—
Product[3-fluoro-4-(1H-pyrazol-1-yl)phenyl]amineHCID 10725981100.6%

Reaction Steps

A suspension of 1-(2-fluoro-4-nitrophenyl)-1H-pyrazole (1.80 g, 8.70 mmol) and Pd—C (10%, 0.200 g) in MeOH (20 mL) (containing 10 drops of 6N HCl) was hydrogenated under balloon H2 overnight. The mixture was filtered through celite. The filtrate was concentrated in vacuo. The residue was dried on vacuum to give 3-fluoro-4-(1H-pyrazol-1-yl)benzenamine as a solid (1.55 g). MS 178.3 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063058B2
Source datasetuspto-grants-2011_11
ORD IDord-3fd49d404bc949c092c67c1e0d49e0b0
Source noteuspto-grants-2011_11