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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1387511Erstellt: 26. Oktober 2026

Benzoyl chloride → N-(4-fluoro-3-nitrophenyl)benzamide

https://huagongshe.com/reaction/1387511

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chlorideHCID 7412—
EduktTriethylamineHCID 8471—
Edukt4-Fluoro-3-nitroanilineHCID 67768—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-(4-fluoro-3-nitrophenyl)benzamideHCID 353522881,1%

Reaktionsschritte

Benzoyl chloride (12 mL, 103 mmol) was added dropwise to 4-fluoro-3-nitroaniline (15.64 g, 100 mmol) and triethylamine (17 mL, 122 mmol) in ethyl acetate (400 mL) at room temperature. The reaction mixture was stirred for 2 hours and then allowed to stand overnight. The reaction mixture was washed with 10% aqueous citric acid solution (200 mL) saturated aqueous sodium bicarbonate solution (200 mL), and brine (100 mL); dried (magnesium sulfate), filtered, and concentrated to about 100 mL at which point a solid began to precipitate. The mixture was cooled to zero degrees and the straw-colored solid collected by filtration to afford the product (21.1 g) in two crops.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06268387B1
Quelldatensatzuspto-grants-2001_07
ORD IDord-9ea7dc66c85f439f8b70aad45b55fe30
Quellennotizuspto-grants-2001_07