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HRID 9524作成日:2026年10月24日

Sodium Hydroxide → Ethyl 4-(4-bromophenyl)-4-oxo-2-(2-phenylethyl)butanoate

https://huagongshe.com/ja/reaction/9524

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Diethyl 2-[2-(4-bromophenyl)-2-oxoethyl]-2-(2-phenylethyl)malonateHCID 21985802—
溶媒AcetoneHCID 180—
溶媒EthanolHCID 702—
生成物Ethyl 4-(4-bromophenyl)-4-oxo-2-(2-phenylethyl)butanoateHCID 2198580565%

反応条件

温度50 °C

反応手順

To a solution of diethyl 2-[2-(4-bromophenyl)-2-oxoethyl]-2-(2-phenylethyl)malonate (7.89 g, 17.1 mmol) in acetone (18.5 mL) and ethanol (17.0 mL) was added 1 N aqueous sodium hydroxide solution (17.1 mL), and the resulting solution was heated at 50° C. for 3 h. Solvent was then removed under reduced pressure via rotary evaporation and the resulting residue was further concentrated under high vacuum for 1 h. The residue was redissolved in dimethoxyethane (18.5 mL) and the solution was heated at 80° C. for 2.5 h. The mixture was cooled to rt, diluted with ethyl acetate, and washed with water. The organic layer was dried over anhydrous sodium sulfate and concentrated under high vacuum. The resulting residue was purified by flash chromatography (Biotage flash 75, 10:90 ethyl acetate/hexane) to afford ethyl 4-(4-bromophenyl)-4-oxo-2-(2-phenylethyl)butanoate (4.32 g, 65%). LC-MS ret. time 3.79 min, m/z 389.2 (MH+); 1H NMR (300 MHz, CDCl3) δ 1.20 (t, 3H), 1.78–1.94 (m, 2H), 2.62 (t, 2H), 2.86–3.01 (m, 2H), 3.26–3.36 (m, 1H), 4.10 (q, 2H), 7.05–7.11 (m, 3H), 7.18–7.23 (m, 2H), 7.51 (d, 2H), 7.72 (d, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091228B2
出典データセットuspto-grants-2006_08
ORD IDord-8fb6d4a6537a45d7bc04373d65cf36ce
出典メモuspto-grants-2006_08