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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1111759생성일: 2026년 10월 24일

Dimethylformamide → 5-Methoxy-3-stilbene carboxylic acid methyl ester

https://huagongshe.com/ko/reaction/1111759

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Diethyl benzylphosphonateHCID 14122—
반응물Sodium hydrideHCID 24758—
반응물HCID 86736055HCID 86736055—
생성물5-Methoxy-3-stilbene carboxylic acid methyl esterHCID 54547754—

반응 단계

To a slurry of 1.0 mole of sodium hydride in 1 liter of N,N-dimethylformamide is added 1.0 mole of diethyl benzylphosphonate. The reaction mixture is stirred for 1 hour and then a solution of 1.0 mole of 3-methoxyisophthalaldehydic acid methyl ester in a minimal amount of dimethylformamide is added. The reaction mixture is stirred for several hours and is then added to ether-water. The ether extract is washed several times with water, dried over magnesium sulfate and evaporated to a residue. The residue is purified via crystallization from hexane to yield 5-methoxy-3-stilbene carboxylic acid methyl ester. The free acid is obtained by refluxing a solution of 1.0 mole of the methyl ester in one liter of 1N methanolic sodium hyroxide for 4-5 hours. The reaction mixture is evaporated to a residue which is added to ethyl acetate. The ethyl acetate solution is extracted with several portions of water. The combined aqueous extract is neutralized with 1N hydrochloric acid and extracted with several portions of ethyl acetate. This organic extract is dried over magnesium sulfate and evaporated to a residue. The residue is purified by crystallization from hexane to yield 5-methoxy-3-stilbene carboxylic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04118559
출처 데이터셋uspto-grants-1978_10
ORD IDord-7ab59022d38b4472bd9f7574cdc1a1c7
출처 메모uspto-grants-1978_10