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HRID 1161403作成日:2026年10月24日

Sodium Iodide → 6-bromo-8-methoxy-4H-benzo[1,3]dioxine

https://huagongshe.com/ja/reaction/1161403

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物BromochloromethaneHCID 6333—
反応物Sodium hydrideHCID 24758—
反応物Ammonium ChlorideHCID 25517—
反応物4-Bromo-2-(hydroxymethyl)-6-methoxyphenolHCID 894092—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物6-bromo-8-methoxy-4H-benzo[1,3]dioxineHCID 59511816—

反応手順

To a solution of the 50 g of 4-bromo-2-hydroxymethyl-6-methoxyphenol in 450 ml of DMF there was added 20 g of sodium hydride (60% oily suspension) while cooling on ice, and the mixture was stirred at room temperature for 30 minutes. After adding 15 ml of bromochloromethane and 3.2 g of sodium iodide to the reaction mixture, it was stirred at 80° C. for 6 hours under a nitrogen atmosphere. Saturated aqueous ammonium chloride was added to the reaction mixture, and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (31.2 g) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07816522B2
出典データセットuspto-grants-2010_10
ORD IDord-35177c5cae3644e08b04824dbc65f47b
出典メモuspto-grants-2010_10