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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400371Generated: October 30, 2026

Hydrogen Bromide → 4-Bromo-1-ethyl-2-nitrobenzene

https://huagongshe.com/reaction/400371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant4-Ethyl-3-nitroanilineHCID 22708680—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product4-Bromo-1-ethyl-2-nitrobenzeneHCID 7566996—

Reaction Conditions

Temperature-5 °C

Reaction Steps

Hydrobromic acid (48% wt. in water, 240 ml) is added dropwise to a suspension of 4-ethyl-3-nitroaniline (20 g, 0.12 mol) in water (80 ml), and the mixture is stirred until the solid dissolves. The mixture is cooled to −5° C. and a solution of sodium nitrite (19.8 g, 0.28 mol) in water (100 ml) is added dropwise, maintaining the temperature at 0-5° C. Once the addition is complete, the cooling bath is removed and the reaction mixture is stirred for one hour at room temperature. The mixture is added dropwise to a pre-cooled solution of cuprous bromide (22.4 g, 0.16 mol) in hydrobromic acid (48% wt. in water) at 0° C. The reaction mixture is stirred and allowed to warm to room temperature over three hours. The mixture is extracted with diethyl ether, and the organic extracts are combined, dried over anhydrous sodium sulfate, filtered and the filtrate is concentrated in vacuo. The residue is further purified by column chromatography on silica gel, eluting with hexane to give 4-bromo-1-ethyl-2-nitrobenzene (18 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741806B2
Source datasetuspto-grants-2014_06
ORD IDord-02c91f9ad526464ca82270c8c7cf6b98
Source noteuspto-grants-2014_06