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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341699Generated: October 26, 2026

Sulfuric Acid → 5-Bromo-1,3-diethyl-2-iodobenzene

https://huagongshe.com/reaction/341699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium IodideHCID 4875—
Reactant4-Bromo-2,6-diethylanilineHCID 611452—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product5-Bromo-1,3-diethyl-2-iodobenzeneHCID 4489110193.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred mixture of 4-bromo-2,6-diethylaniline (13.6 g, 0.06 mol) in distilled water (14 ml) is added concentrated sulphuric acid (14 ml), followed by brief heating to 60° C. for 1 hour until dissolution is complete. The mixture is allowed to cool to room temperature then further cooled to approximately 0° C. in an ice/salt bath. To this slurry is added an aqueous solution of sodium nitrite (4.1 g, 0.059 mol) in distilled water (20 ml) dropwise over 15 minutes, maintaining the temperature below 5° C., followed by additional stirring for 30 minutes. The reaction mixture is allowed to come to room temperature and then a solution of aqueous potassium iodide (29.8 g, 0.18 mol) in distilled water (30 ml) is added 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 (150 ml×3) and the organic phase is washed with 1M aqueous hydrochloric acid (75 ml) and aqueous sodium thiosulfate (2×75 ml). The organic phase is dried over anhydrous sodium sulphate and concentrated under reduced pressure. The residue is purified by column chromatography on silica gel to give 4-bromo-2,6-diethyl-1-iodobenzene (19 g) as an orange liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895761B2
Source datasetuspto-grants-2014_11
ORD IDord-37382491f9124fd38d3e0f5b482ad424
Source noteuspto-grants-2014_11