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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405452Generated: November 3, 2026

4-Bromoaniline → N-(4-bromophenyl)-2-nitroaniline

https://huagongshe.com/reaction/2405452

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanilineHCID 7807—
Reactant1-Bromo-2-nitrobenzeneHCID 11341—
ReactantSodium AcetateHCID 517045—
SolventEthyl AcetateHCID 8857—
ProductN-(4-bromophenyl)-2-nitroanilineHCID 1200029026.2%

Reaction Steps

10 g (49.5 mmol) of 2-bromonitrobenzene, 13 g (163 mmol) of sodium acetate, and 10 g (59 mmol) of 4-bromoaniline were stirred at 180° C. for 8 hours in an argon atmosphere. After cooling the reaction solution to room temperature, the reaction solution was diluted with ethyl acetate, and filtered. After concentrating the filtrate, the residue was washed with methanol to obtain 3.8 g of (4-bromophenyl)-(2-nitrophenyl)amine as an orange crystal (yield: 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08803420B2
Source datasetuspto-grants-2014_08
ORD IDord-087beb95ae97492fbda61fd321ad42c7
Source noteuspto-grants-2014_08