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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1847402Generated: October 30, 2026

4-Nitroaniline → Benzenamine, 2-bromo-4-nitro-

https://huagongshe.com/reaction/1847402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitroanilineHCID 7475—
ReactantBromineHCID 24408—
SolventAcetic AcidHCID 176—
ProductBenzenamine, 2-bromo-4-nitro-HCID 2584072%

Reaction Steps

To a solution of 4-nitroaniline (50 g, 0.36 mol) in AcOH (500 mL) was added liquid Br2 (60 g, 0.38 mol) dropwise at 5° C. The mixture was stirred for 30 min at that temperature. The insoluble solid was collected by filtration and poured into EtOAc (200 mL). The mixture was basified with saturated aqueous NaHCO3 to pH 7. The organic layer was separated. The aqueous phase was extracted with EtOAc (300 mL×3). The combined organic layers were dried and evaporated under reduced pressure to give 2-bromo-4-nitroaniline (56 g, 72%), which was directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952050B2
Source datasetuspto-grants-2015_02
ORD IDord-5509b110b11642c9bec03b6d3d7068b1
Source noteuspto-grants-2015_02