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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49826Erstellt: 23. Oktober 2026

Ethanol → Ethyl (4-acetyl-2-nitrophenyl)aminobenzoate

https://huagongshe.com/de/reaction/49826

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktTriethylamineHCID 8471—
EduktEthyl 3-aminobenzoateHCID 11400—
Edukt4'-Fluoro-3'-nitroacetophenoneHCID 2734612—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktEthyl (4-acetyl-2-nitrophenyl)aminobenzoateHCID 53953856938,3%

Reaktionsschritte

A mixture 1b (11.0 g, 60.2 mmol), ethyl 3-aminobenzoate (9.9 g, 6.2 mmol) and triethylamine (8.34 ml, 60.2 mmol) in anhydrous NMP (5 ml) was heated to 130° C. with stirring under a stream of nitrogen for 4 hours. The cooled mixture was poured into ice-water (100 ml). Ethanol (10 ml) was added and the mixture was stirred until crystallization was completed. The precipitate was filtered off, washed with water and dried to yield ethyl (4-acetyl-2-nitrophenyl)aminobenzoate (19.1 g, 97%). This ester was hydrogenated quantitatively in a mixture of ethanol (400 ml) and dichloromethane (100 ml) using Pd (5% on activated carbon) as the catalyst. The resulting diamine was heated to reflux in formic acid (100 ml) for 1 hour. The cooled mixture was poured into ice-water (400 ml) and the precipitate was filtered off, washed with water and dried to yield 5-acetyl-1-(3-ethoxycarbonyl)phenylbenzimidazole (16.4 g, 91%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710044B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-624de12a3733497c8932b4e4bb825d7e
Quellennotizuspto-grants-2004_03