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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238608생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/238608

반응식

참여 물질

역할이름HCID투입량
반응물4-ChlorobenzaldehydeHCID 7726—
반응물Sodium HydroxideHCID 14798—
반응물Butanedioic acid, 2-methyl-, 1,4-dimethyl esterHCID 15350—
반응물Sodium hydrideHCID 24758—
용매MethanolHCID 887—
용매TolueneHCID 1140—
생성물2-(4-Chloro-benzylidene)-3-methyl-succinic acidHCID 6730420026.3%

반응 단계

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 adding 2 N sodium hydroxide (200 mL) dropwise, then heated to 80° C., and stirred at the same temperature for 2 hours. After being cooled to room temperature naturally, 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642629B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-a0f2adc394ca490f87771b901d954ca3
출처 메모uspto-grants-2014_02