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HRID 747458作成日:2026年10月26日

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

https://huagongshe.com/reaction/747458

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US07396848B1
出典データセットuspto-grants-2008_07
ORD IDord-1e793f0b562b41f9afba3943552c21d5
出典メモuspto-grants-2008_07