反応式
[OH:1][C:2]1[C:7]2[CH:8]=[CH:9][O:10][C:6]=2[CH:5]=[CH:4][CH:3]=1.Br[CH2:12][C:13]1[CH:23]=[CH:22][C:16]([C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:15][CH:14]=1.C(=O)([O-])[O-].[K+].[K+].[I-].[Na+]>[OH-].[Na+].C(O)C>[O:10]1[C:6]2[CH:5]=[CH:4][CH:3]=[C:2]([O:1][CH2:12][C:13]3[CH:23]=[CH:22][C:16]([C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:15][CH:14]=3)[C:7]=2[CH:8]=[CH:9]1参加物
7
実験手順
4-Hydroxybenzofuran (1.34 g, 0.01 M), ethyl 4-bromomethylbenzoate (2.43 g, 0.01 M), anhydrous potassium carbonate (1.49 g), sodium iodide (0.05 g) and 95% ethanol (10 ml) were refluxed with stirring (5 hr). The cooled reaction mixture was diluted with 0.5 N sodium hydroxide solution and cooled in ice. The precipitated solid was filtered off, washed well with water and recrystallised form ethanol-water to give ethyl 4-(4-benzofuranyloxymethyl)benzoate, m.p. 70°-72° C. (Found: C, 72.79; H, 5.46. C18H16O4 requires C, 72.96; H, 5.44%).
後処理
- customThe cooled reaction mixture
- temperaturecooled in ice
- filtrationThe precipitated solid was filtered off
- washwashed well with water
- customrecrystallised
- customform ethanol-water
出典と根拠
- ORDレコード
- ord-aba515183f024d00a5a792158bb69827
- 出典データセット
- uspto-grants-1985_08
- 特許番号
- US04535183
関連ノート
読み込み中…