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HRID 2220439作成日:2026年10月25日

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

https://huagongshe.com/reaction/2220439

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US07417047B2
出典データセットuspto-grants-2008_08
ORD IDord-81eb66d0faf046609e9bbb330e8d1602
出典メモuspto-grants-2008_08