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HRID 1111759作成日:2026年10月25日

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

https://huagongshe.com/reaction/1111759

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HCID 86736055HCID 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 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04118559
出典データセットuspto-grants-1978_10
ORD IDord-7ab59022d38b4472bd9f7574cdc1a1c7
出典メモuspto-grants-1978_10