反応式
[H-].[Na+].[CH2:3](P(=O)(OCC)OCC)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH3:18][O:19][C:20](=[O:31])[C:21]1[CH2:22][C:23]([O:29][CH3:30])([CH:26]=[CH:27][CH:28]=1)C=O.[CH3:32]N(C)C=O>>[CH3:18][O:19][C:20]([C:21]1[CH:28]=[C:27]([CH:32]=[CH:3][C:4]2[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:26]=[C:23]([O:29][CH3:30])[CH:22]=1)=[O:31]参加物
実験手順
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.
後処理
- stirringThe reaction mixture is stirred for several hours
- extractionThe ether extract
- washis washed several times with water
- dry with materialdried over magnesium sulfate
- customevaporated to a residue
- customThe residue is purified via crystallization from hexane
出典と根拠
- ORDレコード
- ord-7ab59022d38b4472bd9f7574cdc1a1c7
- 出典データセット
- uspto-grants-1978_10
- 特許番号
- US04118559
関連ノート
読み込み中…