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HRID 341702Erstellt: 25. Oktober 2026

Sulfuric Acid → 5-Bromo-2-iodo-1,3-dimethylbenzene

https://huagongshe.com/reaction/341702

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktPotassium IodideHCID 4875—
Edukt4-Bromo-2,6-xylidineHCID 90549—
EduktSodium NitriteHCID 23668193—
LösungsmittelWaterHCID 962—
Produkt5-Bromo-2-iodo-1,3-dimethylbenzeneHCID 273557365,2%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a stirred mixture of 4-bromo-2,6-dimethylaniline (75 g, 0.37 mol) in distilled water (75 ml) is added concentrated sulphuric acid (75 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 (25.33 g, 0.36 mol) in distilled water (126 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 (187.6 g, 1.13 mol) in distilled water (190 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 (750 ml×3) and the organic phase is washed with 1M aqueous hydrochloric acid (200 ml) and aqueous sodium thiosulfate (2×200 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-dimethyl-1-iodo benzene (75 g) as an orange liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895761B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-0d89030a099e400a84015b8ec7853607
Quellennotizuspto-grants-2014_11