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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 341702생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/341702

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Potassium IodideHCID 4875—
반응물4-Bromo-2,6-xylidineHCID 90549—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
생성물5-Bromo-2-iodo-1,3-dimethylbenzeneHCID 273557365.2%

반응 조건

온도60 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895761B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-0d89030a099e400a84015b8ec7853607
출처 메모uspto-grants-2014_11