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HRID 1460892생성일: 2026년 10월 24일

Iodine → (4-Methoxyphenyl)(3-methylphenyl)methanone

https://huagongshe.com/ko/reaction/1460892

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Sulfuric AcidHCID 1118—
반응물3-BromotolueneHCID 11560—
반응물4-MethoxybenzonitrileHCID 70129—
반응물MagnesiumHCID 5462224—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물(4-Methoxyphenyl)(3-methylphenyl)methanoneHCID 1246946673.5%

반응 단계

A 3-neck flask equipped with a condenser, mechanical stirrer and dropping funnel is charged under nitrogen with 1.925 g (79.19 g.a.) of magnesium turnings and enough ether to cover the turnings. A few drops of a solution of 3-bromotoluene (15.79 g, 92.28 mmole) in ether (40 mL) is then added along with a crystal of iodine to initiate the reaction. The remainder of the solution is then added dropwise and the mixture is refluxed until most of the magnesium has disappeared. After cooling, a solution of 4-methoxybenzonitrile (10 g, 75.1 mmole, dried in vacuo over P2O5) is added in one portion. The mixture is refluxed for 2 hours (TLC, no starting material present), cooled (ice bath) and slowly treated with cold water (130 mL) followed by dilute H2SO4 (1:1, v/v, 25 mL). The decomposition of the complex is completed by refluxing the mixture for 4 hours (followed by TLC, 8:2 ether-ethyl acetate). Following stirring overnight at room temperature, the layers are separated and extracted with ether (3×). The extracts are washed with 5% NaHCO3, dried (MgSO4) and evaporated to dryness. The crude material (amber oil, 13.93 g) is purified by flash chromatography (on silica Merck-60, eluted with 8:2 petrolether-ethyl acetate) to provide the title compound as a light yellow oil (12.5 g, 73.5%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05071988
출처 데이터셋uspto-grants-1991_12
ORD IDord-6522bed826884085b5f2d73643f7e73c
출처 메모uspto-grants-1991_12