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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 427602Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/427602

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
PatentnummerUS06313122B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-4e3ffc13d5264bc4bc9ada48cfeaba5f
Quellennotizuspto-grants-2001_11