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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575994Generated: October 25, 2026

Ethyl Acetate → 2-Bromo-5-fluoro-4-nitroaniline

https://huagongshe.com/reaction/575994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantN-bromobutanimideHCID 67184—
Reactant3-Fluoro-4-nitroanilineHCID 75401—
SolventDimethyl SulfoxideHCID 679—
Product2-Bromo-5-fluoro-4-nitroanilineHCID 5748851350%

Reaction Conditions

Temperature22 °C

Reaction Steps

A flask was charged with 3-fluoro-4-nitroaniline (1.0 equiv) followed by ethyl acetate (10 vol) and stirred to dissolve all solids. N-Bromosuccinimide (1.0 equiv) was added as a portion-wise as to maintain internal temperature of 22° C. At the end of the reaction, the reaction mixture was concentrated in vacuo on a rotavap. The residue was slurried in distilled water (5 vol) to dissolve and remove succinimide. (The succinimide can also be removed by water workup procedure.) The water was decanted and the solid was slurried in 2-propanol (5 vol) overnight. The resulting slurry was filtered and the wetcake was washed with 2-propanol, dried in vacuum oven at 50° C. overnight with N2 bleed until constant weight was achieved. A yellowish tan solid was isolated (50% yield, 97.5% AUC). Other impurities were a bromo-regioisomer (1.4% AUC) and a di-bromo adduct (1.1% AUC). 1H NMR (500 MHz, DMSO)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09035072B2
Source datasetuspto-grants-2015_05
ORD IDord-ffd44fb689384bbbaebea332048aa6b4
Source noteuspto-grants-2015_05