Citric Acid → HCID 10792589、化合物
反応式
[O:1]1[CH:5]=[CH:4][C:3]2[CH:6]=[C:7]([CH2:10][CH2:11][C:12]([C:14]3[C:19]([OH:20])=[CH:18][C:17]([CH3:21])=[CH:16][C:15]=3[O:22][C@@H:23]3[O:31][C@H:30]([CH2:32][OH:33])[C@@H:28]([OH:29])[C@H:26]([OH:27])[C@H:24]3[OH:25])=[O:13])[CH:8]=[CH:9][C:2]1=2.C(N(CC)CC)C.[C:41](Cl)(=[O:43])[CH3:42].C(O)(=O)[CH2:46][C:47](CC(O)=O)(C(O)=O)[OH:48]>CN(C)C(=O)C>[O:1]1[CH:5]=[CH:4][C:3]2[CH:6]=[C:7]([CH2:10][CH2:11][C:12]([C:14]3[C:19]([O:20][C:41](=[O:43])[CH3:42])=[CH:18][C:17]([CH3:21])=[CH:16][C:15]=3[O:22][C@@H:23]3[O:31][C@H:30]([CH2:32][O:33][C:47](=[O:48])[CH3:46])[C@@H:28]([OH:29])[C@H:26]([OH:27])[C@H:24]3[OH:25])=[O:13])[CH:8]=[CH:9][C:2]1=2参加物
実験手順
3-(5-Benzo[b]furanyl)-2'-(β-D-glucopyranosyloxy)-6'-hydroxy-4'-methylpropiophenone (500 mg) is dissolved in N,N-dimethylacetamide (3.5 ml), and thereto is added triethylamine (315 mg). To the mixture is added dropwise acetyl chloride (282 mg) under ice-cooling, and the mixture is stirred under ice-cooling for 30 minutes, and stirred at room temperature overnight. The reaction mixture is poured into chilled 10% aqueous citric acid solution, and extracted with ethyl acetate. The organic layer is washed with water, dried, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography (solvent; chloroform/methanol) to give 3-(5-benzo[b]-furanyl)-2'-(6-O-acetyl-β-D-glucopyranosyloxy)-6'-acetoxy-4'-methylpropiophenone (304 mg).
後処理
- temperaturecooling
- temperaturecooling for 30 minutes
- stirringstirred at room temperature overnight
- additionThe reaction mixture is poured
- extractionextracted with ethyl acetate
- washThe organic layer is washed with water
- customdried
- concentrationconcentrated under reduced pressure
- customThe residue is purified by silica gel column chromatography (solvent; chloroform/methanol)
出典と根拠
- ORDレコード
- ord-62e821b465464fa2878e9adefd2f4229
- 出典データセット
- uspto-grants-2000_04
- 特許番号
- US06048842
反応ノート
読み込み中…