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HRID 238601作成日:2026年10月23日

Methanol → 2-(4-Fluoro-benzylidene)-3-methyl-succinic acid 1-methyl ester

https://huagongshe.com/ja/reaction/238601

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Butanedioic acid, 2-methyl-, 1,4-dimethyl esterHCID 15350—
反応物Sodium hydrideHCID 24758—
反応物4-FluorobenzaldehydeHCID 68023—
溶媒TolueneHCID 1140—
生成物2-(4-Fluoro-benzylidene)-3-methyl-succinic acid 1-methyl esterHCID 6677558733%

反応手順

After careful addition of absolute methanol (0.1 mL) to a suspension of sodium hydride (60% in mineral oil, 20 g, 0.5 mol) in anhydrous toluene (200 mL), a solution of 4-fluoro-benzaldehyde (31 g, 0.25 mol) and 2-methyl-succinic acid dimethyl ester (60 g, 0.38 mol) in anhydrous toluene (100 mL) was added at room temperature under a stream of nitrogen. The resulting mixture was stirred at room temperature for 30 minutes and then quenched by the slow addition of water (20 mL). The mixture was acidified by the addition of concentrated hydrochloric acid, and extracted with ethyl acetate (200 mL×3). The combined organic layers were dried over sodium sulfate, and concentrated in vacuo. The residue was purified by column chromatography (elution with 30% ethyl acetate in petroleum ether) to afford 2-(4-fluoro-benzylidene)-3-methyl-succinic acid 1-methyl ester (20 g, 33%) as a white solid. 1H NMR (400 MHz, acetone-d6) δ ppm 7.77 (s, 1H), 7.54 (d, J=8.8 Hz, 2H), 7.25 (d, J=8.8 Hz, 2H), 3.82 (q, 7.2 Hz, 1H), 1.40 (d, J=6.8 Hz, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642629B2
出典データセットuspto-grants-2014_02
ORD IDord-cc74954780564f1fbeb84ad8f3fdcd1d
出典メモuspto-grants-2014_02