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HRID 1468332作成日:2026年10月27日

4-Chlorobenzaldehyde → 2-(4-Chloro-benzylidene)-3-methyl-succinic acid

https://huagongshe.com/reaction/1468332

反応式

関与物質

役割名称HCID仕込み量
反応物4-ChlorobenzaldehydeHCID 7726—
反応物Sodium HydroxideHCID 14798—
反応物Butanedioic acid, 2-methyl-, 1,4-dimethyl esterHCID 15350—
反応物Sodium hydrideHCID 24758—
溶媒MethanolHCID 887—
溶媒TolueneHCID 1140—
生成物2-(4-Chloro-benzylidene)-3-methyl-succinic acidHCID 6730420026.3%

反応手順

After careful addition of absolute methanol (0.1 mL) to a suspension of sodium hydride (60% in mineral oil, 16 g, 0.40 mol) in anhydrous toluene (200 mL), a solution of 4-chloro-benzaldehyde (28 g, 0.20 mol) and 2-methyl-succinic acid dimethyl ester (48 g, 0.30 mol) in anhydrous toluene (100 mL) was added dropwise at room temperature under a stream of nitrogen. After being stirred at room temperature for 2 hours, the resulting mixture was diluted by addition of 2 N sodium hydroxide (200 mL) dropwise. The mixture was heated to 80° C., and stirred at this temperature for 2 hours. After cooling to room temperature, the aqueous layer was separated, washed with ethyl acetate (100 mL×3), then acidified with 2 N hydrochloric acid to pH 2 and extracted with ethyl acetate (150 mL×3). The combined organic layers were dried over sodium sulfate, and concentrated in vacuo. The residue was precipitated from ethyl acetate/petroleum ether (10:1) to give 2-(4-chloro-benzylidene)-3-methyl-succinic acid (13.4 g, 26%) as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09000044B2
出典データセットuspto-grants-2015_04
ORD IDord-5c6b560faa0d45859ddc45367b794e1b
出典メモuspto-grants-2015_04