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HRID 747457作成日:2026年10月26日

Bromine → Ethyl 5-bromo-6-(4-fluoro-1-naphthyl)-6-oxohexanoate

https://huagongshe.com/reaction/747457

反応式

関与物質

役割名称HCID仕込み量
反応物BromineHCID 24408—
反応物Sodium SulfiteHCID 24437—
反応物Ethyl 6-(4-fluoro-1-naphthyl)-6-oxohexanoateHCID 18174724—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 5-bromo-6-(4-fluoro-1-naphthyl)-6-oxohexanoateHCID 18174722—

反応手順

Ethyl 6-(4-fluoro-1-naphthyl)-6-oxohexanoate (27.7 g) was dissolved in methylene chloride (100 ml), and bromine (14.6 g) was added dropwise with stirring at room temperature. After an hour of stirring at room temperature, a 10% aqueous solution of sodium sulfite was carefully added until disappearance of the red color of bromine, which was extracted with diethyl ether (300 ml×2). The organic layer was washed with a 10% aqueous solution of sodium hydrogen carbonate (100 ml), dried over anhydrous magnesium sulfate, and concentrated to give ethyl 5-bromo-6-(4-fluoro-1-naphthyl)-6-oxohexanoate as an oil (34.9 g, quantitative).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07396848B1
出典データセットuspto-grants-2008_07
ORD IDord-f9d587e51908422b99d73dcfb3ce2c6e
出典メモuspto-grants-2008_07