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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246751Generated: October 26, 2026

3-fluoro-N-(2-fluorophenyl)-2-nitroaniline → 3-fluoro-N1-(2-fluorophenyl)benzene-1,2-diamine

https://huagongshe.com/reaction/2246751

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-fluoro-N-(2-fluorophenyl)-2-nitroanilineHCID 55100410—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-fluoro-N1-(2-fluorophenyl)benzene-1,2-diamineHCID 6078894038%

Reaction Steps

To 2-fluoroaniline (1.55 g, 13.9 mmol) in anhydrous dimethylformamide (10 mL) was added sodium hydride (0.56 g, 13.9 mmol) and the reaction stirred for 10 minutes prior to the addition of 2,6-difluoronitrobenzene (2 g, 15.5 mmol) dissolved in anhydrous dimethylformamide (2 mL). Upon disappearance of 2-fluoroaniline the reaction was partitioned between saturated ammonium chloride (50 mL) and ethyl acetate (50 mL) and the organics were dried over sodium sulfate. The product was purified on silica gel using the ISCO (0-70% ethyl acetate/hexane) to give (3-Fluoro-2-nitro-phenyl)-(2-fluoro-phenyl)-amine as a slightly impure off-white solid (1.5 g, 43%). (3-Fluoro-2-nitro-phenyl)-(2-fluoro-phenyl)-amine (1.5 g, 6 mmol) and a spatula tip of 5% Pd/C in methanol (100 mL) were reduced in the parr shaker. Upon complete reduction, the reaction was filtered through a pad of celite and concentrated onto silica gel. The product was purified on silica gel using the ISCO (0-70% ethyl acetate/hexane) to give 3-fluoro-N1-(2-fluorophenyl)benzene-1,2-diamine as a brown oil (0.5 g, 38%). MS (ES) m/z 221.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687529B2
Source datasetuspto-grants-2010_03
ORD IDord-d6843c5ec05f4cd890b1046fbf277188
Source noteuspto-grants-2010_03