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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395751Generated: October 25, 2026

N-(4-fluorophenyl)-2-nitrobenzamide → 2-amino-N-(4-fluorophenyl)benzamide

https://huagongshe.com/reaction/395751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-fluorophenyl)-2-nitrobenzamideHCID 691037—
ReactantSodium borohydrideHCID 4311764—
CatalystNickel acetate tetrahydrateHCID 62601—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product2-amino-N-(4-fluorophenyl)benzamideHCID 47882281%

Reaction Steps

To a stirred solution of N-(4-fluorophenyl)-2-nitrobenzamide (4.0 g, 15.4 mmol) in methanol (220 mL) and tetrahydrofuran (110 mL) was added nickel acetate tetrahydrate (7.7 g, 31 mmol). Sodium borohydride (2.3 g, 62 mmol) was added in small portions. After gas evolution had ceased, the solvent was removed in vacuo. The residue was partitioned between ethyl acetate and concentrated ammonium hydroxide, and the layers were separated. The organic phase was washed with concentrated ammonium hydroxide and saturated aqueous sodium chloride solution, dried (magnesium sulfate), filtered, and concentrated in vacuo to give 2.86 g (81%) of the title compound as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605626B2
Source datasetuspto-grants-2003_08
ORD IDord-9ead5ee5720c457daaeaa252346062d3
Source noteuspto-grants-2003_08