Vanillin → 1-(4'-Hydroxy,3'-methoxyphenyl)-4-phenyl-1-butene-3-one
反応式
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][C:3]=1[O:10][CH3:11].C1([PH2]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)C2C=CC=CC=2)C=CC=CC=1.[O:31](CC(=O)C)[C:32]1[CH:37]=CC=C[CH:33]=1>C1(C)C=CC=CC=1.C(OCC)(=O)C>[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[CH:33][C:32](=[O:31])[CH2:37][C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=2)=[CH:4][C:3]=1[O:10][CH3:11]参加物
実験手順
4-Hydroxy-3-methoxybenzaldehyde (2.1 g, 13.8 mMol) and 3-phenoxypropane-2-one triphenylphosphorane (2.8 g, 6.9 mMol) (prepared as described by LeCorre: C. R. Acad. Sci. Paris 273 81 (1971)) are dissolved in 100 ml of toluene and warmed to reflux. After three hours, the solvent is evaporated and the residue is taken up in tHF. Sodium bisulfite (10.0 g) is dissolved in 100 ml of water and stirred with the solution for one hour. The THF is evaporated and the water is extracted with chloroform. Drying over magnesium sulfate and evaporation of the chloroform gives a yellow oil. Flash chromatography in ethyl acetate on silica gel gives 1.5 g (65%) of 1-(4'-hydroxy,3'-methoxyphenyl)-4-phenyl-1-butene-3-one; mp=85°-87° C. C, H analysis: Calcd for C17H16O4 (71.81, 5.68); Found (71.85, 5.50).
後処理
- temperaturewarmed to reflux
- customthe solvent is evaporated
- dissolutionSodium bisulfite (10.0 g) is dissolved in 100 ml of water
- customThe THF is evaporated
- extractionthe water is extracted with chloroform
- dry with materialDrying over magnesium sulfate and evaporation of the chloroform
- customgives a yellow oil
出典と根拠
- ORDレコード
- ord-76a03d7971514bcdbf854d0267151164
- 出典データセット
- uspto-grants-1992_08
- 特許番号
- US05142095
反応ノート
読み込み中…