Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487411Generated: October 25, 2026

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

https://huagongshe.com/reaction/487411

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromobenzoic acidHCID 6940—
Reactant4-NitroanilineHCID 7475—
ReactantThionyl ChlorideHCID 24386—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-bromo-N-(4-nitrophenyl)benzamideHCID 521255587%

Reaction Conditions

Temperature80 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05294716
Source datasetuspto-grants-1994_03
ORD IDord-9a0bfd21d74c463aa22299849bce18a8
Source noteuspto-grants-1994_03