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HRID 1022463作成日:2026年10月27日

1,4-Benzodioxan → Methanone, (2-bromo-5-iodophenyl)(2,3-dihydro-1,4-benzodioxin-6-yl)-

https://huagongshe.com/reaction/1022463

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-BenzodioxanHCID 10301—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物2-Bromo-5-iodobenzoyl chlorideHCID 58340809—
溶媒DichloromethaneHCID 6344—
生成物Methanone, (2-bromo-5-iodophenyl)(2,3-dihydro-1,4-benzodioxin-6-yl)-HCID 5834079888.5%

反応手順

To a stirred solution of 2-bromo-5-iodo-benzoyl chloride (−158 g, 457 mmol) in DCM (1500 ml) was added benzo(1,4)-dioxane (65.8 ml, 549 mmol) at 0° C. To this reaction mixture, aluminum chloride (195.4 g, 1465 mmol) was added in portions. After stirring for overnight at room temperature, reaction mixture was poured into crushed ice. This was extracted with dichloromethane (1000 ml×2). Dichloromethane layer was washed with water (1000 ml), saturated aqueous sodium bicarbonate solution (1000 ml×2), brine (1000 ml), dried over sodium sulfate, and concentrated. The solid product was triturated with hexanes. The product was dried under vacuum to give 180 g of (2-bromo-5-iodo-phenyl)-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-methanone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08722633B2
出典データセットuspto-grants-2014_05
ORD IDord-ef8c683df2d84731829d59d691fc2805
出典メモuspto-grants-2014_05