戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 225183作成日:2026年10月26日

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

https://huagongshe.com/reaction/225183

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Diethyl benzylphosphonateHCID 14122—
反応物Sodium hydrideHCID 24758—
反応物3-Methoxyisophthalaldehydic acid methyl esterHCID 86736055—
生成物5-Methoxy-3-stilbene carboxylic acid methyl esterHCID 54547754—

反応手順

To a slurry of 1.0 mole of sodium hydride in one liter of N,N-dimethylformamide is added 1.0 mole of diethyl benzylphosphonate. The reaction mixture is stirred for one 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 1 N methanolic sodium hydroxide 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 1 N 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04235913
出典データセットuspto-grants-1980_11
ORD IDord-70f5cfcf297b4dba9e4b1d43b17bba4a
出典メモuspto-grants-1980_11