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HRID 339473作成日:2026年10月23日

Potassium Iodide → 5-Bromo-2-cyclopropyliodobenzene

https://huagongshe.com/ja/reaction/339473

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Sodium BicarbonateHCID 516892—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物Sodium PyrosulfiteHCID 656671—
反応物5-Bromo-2-cyclopropylanilineHCID 4712248—
反応物Sodium NitriteHCID 23668193—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物5-Bromo-2-cyclopropyliodobenzeneHCID 58061571—

反応手順

5-Bromo-2-cyclopropylaniline (4.74 g) is added to a solution of para-toluene sulfonic acid monohydrate (12.2 g, 0.064 mol) in acetonitrile (130 ml), followed by stirring for 10 minutes at room temperature. The suspension is then cooled to 10° C. and a mixed solution of sodium nitrite (8.9 g, 0.054 mol) and potassium iodide (3.1 g, 0.044 mol) in water (16 ml) is added dropwise over 30 minutes. Once the addition is complete the reaction mixture is allowed to stir at 10° C. for 20 minutes and then at room temperature for 4 hours. The reaction mixture is basified to pH 9-10 with aqueous sodium bicarbonate, followed by addition of ethyl acetate and 10% aqueous sodium metabisulphite. The phases are separated and the aqueous layer is extracted again with ethyl acetate (×2). Organics are combined, washed with brine, dried over magnesium sulfate then concentrated in vacuo to give the crude product which is purified by flash column chromatography on silica gel (isohexane eluant) to afford 5-bromo-2-cyclopropyliodobenzene as a colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895474B2
出典データセットuspto-grants-2014_11
ORD IDord-74d8fe0a3fc6466c991119e3a704d4c9
出典メモuspto-grants-2014_11