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HRID 339473생성일: 2026년 10월 23일

Potassium Iodide → 5-Bromo-2-cyclopropyliodobenzene

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Sodium BicarbonateHCID 516892—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물Sodium PyrosulfiteHCID 656671—
반응물5-Bromo-2-cyclopropylanilineHCID 4712248—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물5-Bromo-2-cyclopropyliodobenzeneHCID 58061571—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895474B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-74d8fe0a3fc6466c991119e3a704d4c9
출처 메모uspto-grants-2014_11