戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 341699作成日:2026年10月26日

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

https://huagongshe.com/reaction/341699

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物Potassium IodideHCID 4875—
反応物4-Bromo-2,6-diethylanilineHCID 611452—
反応物Sodium NitriteHCID 23668193—
溶媒WaterHCID 962—
生成物5-Bromo-1,3-diethyl-2-iodobenzeneHCID 4489110193.4%

反応条件

温度60 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895761B2
出典データセットuspto-grants-2014_11
ORD IDord-37382491f9124fd38d3e0f5b482ad424
出典メモuspto-grants-2014_11