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HRID 646217作成日:2026年10月27日

Water → 1-(3-bromophenyl)-2-(1H-pyrrol-3-yl)ethane-1,2-dione

https://huagongshe.com/reaction/646217

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物Potassium PermanganateHCID 516875—
反応物Sodium BicarbonateHCID 516892—
反応物3-[(3-bromophenyl)ethynyl]-1-(triisopropylsilyl)-1H-pyrroleHCID 68700899—
溶媒AcetoneHCID 180—
生成物1-(3-bromophenyl)-2-(1H-pyrrol-3-yl)ethane-1,2-dioneHCID 5977266842%

反応手順

To a solution of 3-[(3-bromophenyl)ethynyl]-1-(triisopropylsilyl)-1H-pyrrole (2.7 g, 8.5 mmol) in acetone (100 mml) is added a solution of MgSO4 (1.53 g, 12.75 mmol) and NaHCO3 (316 mg, 3.76 mmol) in water (50 ml), followed by the addition of KMnO4 (2.68 g, 17 mmol) in one portion at room temperature. After refluxing for 5 h, the reaction mixture is cooled to room temperature and extracted with ether (2×50 mL), the combined organic extracts are dried over MgSO4. The crude material is purified flash chromatography (silica gel, EtOAc/hexane:30/70 to 50/50) to afford the title compound as a yellow solid (42%). mp: 111-113° C. MS (−) ES: 276 (M−H)−.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07705030B2
出典データセットuspto-grants-2010_04
ORD IDord-1ff6724febe040d7a3ca943bfb82992f
出典メモuspto-grants-2010_04