関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Diethyl benzylphosphonate | HCID 14122 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 3-Methoxyisophthalaldehydic acid methyl ester | HCID 86736055 | — |
| 生成物 | 5-Methoxy-3-stilbene carboxylic acid methyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04235913 |
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| 出典データセット | uspto-grants-1980_11 |
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| ORD ID | ord-70f5cfcf297b4dba9e4b1d43b17bba4a |
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| 出典メモ | uspto-grants-1980_11 |
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