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HRID 395663作成日:2026年10月25日

Methanol → Ethyl 6-(4-fluoro-1-naphthyl)-5-hydroxy-6-oxohexanoate

https://huagongshe.com/reaction/395663

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Sodium FormateHCID 2723810—
反応物Ethyl 5-bromo-6-(4-fluoro-1-naphthyl)-6-oxohexanoateHCID 18174722—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 6-(4-fluoro-1-naphthyl)-5-hydroxy-6-oxohexanoateHCID 18174704—

反応手順

A mixture of ethyl 5-bromo-6-(4-fluoro-1-naphthyl)-6-oxohexanoate (34.3 g), sodium formate (34.0 g) and methanol (150 ml) was stirred with heating under reflux for 16 hours. The reaction mixture was diluted with ethyl acetate (500 ml) and washed with water (200 ml×2). The organic layer was dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography, and ethyl 6-(4-fluoro-1-naphthyl)-5-hydroxy-6-oxohexanoate was obtained as a yellow oil (19.0 g, 65%) from an ethyl acetate-hexane (1:4, v/v)-eluted fraction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06605629B1
出典データセットuspto-grants-2003_08
ORD IDord-efb4936ba28c428d8cd2e3ca784b8740
出典メモuspto-grants-2003_08