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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191553Generated: November 1, 2026

Sulfuric Acid → 4-Bromo-1-ethyl-2-iodobenzene

https://huagongshe.com/reaction/1191553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium IodideHCID 4875—
Reactant5-Bromo-2-ethylanilineHCID 23346756—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product4-Bromo-1-ethyl-2-iodobenzeneHCID 59445913—

Reaction Steps

To a stirred mixture of 5-bromo-2-ethylaniline (3.39 g, 200 mmol) in distilled water (110 ml) is added concentrated sulfuric acid (5.60 ml), followed by brief heating at reflux until dissolution. The mixture is allowed to cool to room temperature, producing a fine precipitate, then further cooled to approximately 0° C. in an ice/salt bath. To this slurry is added an aqueous solution of sodium nitrite (1.17 g, 16.94 mmol) in distilled water (10 ml) dropwise over 15 minutes, maintaining a temperature below 5° C., followed by additional stirring for 30 minutes. The reaction mixture is next filtered then added to a second solution of aqueous potassium iodide (8.44 g, 50.83 mmol) in distilled water (45 ml) dropwise at room temperature. After the addition is complete the solution is briefly heated to 80° C. then allowed to cool to room temperature again. The reaction mixture is extracted with ethyl acetate (3×50 ml), and the organic phase is washed with 1M aqueous hydrochloric acid (30 ml) and aqueous sodium thiosulfate (2×30 ml). After drying over anhydrous magnesium sulfate and concentration in vacuo 4-bromo-1-ethyl-2-iodobenzene (4.90 g) is furnished as an orange liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680012B2
Source datasetuspto-grants-2014_03
ORD IDord-6c0a63d4532840dd9b9cc4d56fb137b9
Source noteuspto-grants-2014_03