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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 395751Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/395751

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-(4-fluorophenyl)-2-nitrobenzamideHCID 691037—
EduktSodium borohydrideHCID 4311764—
KatalysatorNickel acetate tetrahydrateHCID 62601—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-amino-N-(4-fluorophenyl)benzamideHCID 47882281%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06605626B2
Quelldatensatzuspto-grants-2003_08
ORD IDord-9ead5ee5720c457daaeaa252346062d3
Quellennotizuspto-grants-2003_08