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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 605225Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/605225

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chlorideHCID 7412—
EduktTriethylamineHCID 8471—
Edukt4-Fluoro-3-nitroanilineHCID 67768—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(4-fluoro-3-nitrophenyl)benzamideHCID 353522881,1%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

To a solution of 4-fluoro-3-nitroaniline (2.00 g, 12.8 mmol) and Et3N (1.98 mL, 14.1 mmol) in THF (40 mL) was added benzoyl chloride (1.58 ml, 13.5 mmol) dropwise at 5° C. The mixture was stirred at 5° C. for 1 hour, warmed to room temperature, and then evaporated. The residue was suspended in H2O (100 ml), adjusted to pH 2, and then extracted with EtOAc. The extract was washed with H2O, 10% NaHCO3 and brine, dried over MgSO4, and concentrated under vacuum to give the crude product, which was purified by washing with i-Pr2O to give the title compound as pale brown crystal (2.70 g, 81%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07910595B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-fc9411b66fab42c6a4fae27770980d1c
Quellennotizuspto-grants-2011_03