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HRID 37614Erstellt: 23. Oktober 2026

2-Bromobenzoic acid → 2-bromo-N-(4-nitrophenyl)benzamide

https://huagongshe.com/de/reaction/37614

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Bromobenzoic acidHCID 6940—
Edukt4-NitroanilineHCID 7475—
EduktThionyl ChlorideHCID 24386—
LösungsmittelTolueneHCID 1140—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt2-bromo-N-(4-nitrophenyl)benzamideHCID 521255587%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Thionyl chloride (120.5 g) was added to a stirred mixture of 2-bromobenzoic acid (194 g) in toluene (500 ml) and N,N-dimethylformamide (DMF) (5 ml) and the mixture heated at 80° C. for 4 hours. The solution was cooled to 20° C. and added slowly to a solution of 4-nitroaniline (133.1 g) in toluene (500 ml) and NMP (120 ml), maintaining the temperature of the reaction mixture between 20°-25° C. The reaction mixture was then stirred for 24 hours when a solid precipitated. Water (360 ml) was added with rigorous stirring and the suspended solid collected by filtration, and washed successively with water, toluene and acetonitrile to give 2-bromo-N-(4-nitrophenyl)benzamide (B) as a solid, in 87% yield; m.p. 200°-202° C.; NMR(d6 -DMSO): 7.4-7.8(m, 7H), 8.0(d, 2H), 8.3(d, 2H), 11.5(brs, 1H); which was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05420292
Quelldatensatzuspto-grants-1995_05
ORD IDord-542d0b8c5cb74239920d2a30bd1d47ab
Quellennotizuspto-grants-1995_05