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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197784Generated: November 2, 2026

4-Bromoaniline → N-(4-bromophenyl)-4-chloro-3-nitrobenzamide

https://huagongshe.com/reaction/2197784

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanilineHCID 7807—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Chloro-3-nitrobenzoyl chlorideHCID 123477—
SolventDichloromethaneHCID 6344—
ProductN-(4-bromophenyl)-4-chloro-3-nitrobenzamideHCID 1068537—

Reaction Steps

A mixture of 4-bromoaniline (2.58 g 14.99 mmol) in dry CH2Cl2 (100 mL) was treated with 4-chloro-3-nitrobenzoyl chloride (3.60 g, 17.99 mmol) and N,N-diisopropyl-ethylamine (3.14 mL, 17.99 mmol), and the resulting mixture stirred at room temperature for 17 hours. The solvent was concentrated under vacuum giving the title compound and the residue taken up in ethyl acetate (100 mL) and washed with water and brine. The organic extract was dried over Na2SO4, filtered and concentrated under vacuum giving the title compound as a tan solid (5.132 g, 14.45 mmol, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338605B2
Source datasetuspto-grants-2012_12
ORD IDord-fb390fc8fc774d83919bc139d22bbc03
Source noteuspto-grants-2012_12