Ethanol → Ethyl 4-(4-(adamantan-1-yl)phenoxy)butanoate
反応式
[C:1]12([C:11]3[CH:23]=[CH:22][C:14]([O:15][CH2:16][CH2:17][CH2:18][C:19]([OH:21])=[O:20])=[CH:13][CH:12]=3)[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.S(=O)(=O)(O)O.[CH2:29](O)[CH3:30]>>[CH2:29]([O:20][C:19](=[O:21])[CH2:18][CH2:17][CH2:16][O:15][C:14]1[CH:13]=[CH:12][C:11]([C:1]23[CH2:2][CH:3]4[CH2:4][CH:5]([CH2:6][CH:7]([CH2:9]4)[CH2:8]2)[CH2:10]3)=[CH:23][CH:22]=1)[CH3:30]参加物
4
実験手順
1 mol of 4-[4-(1-adamantyl)-phenoxy]-butyric acid is dissolved in excess ethanol and boiled, with addition of 3% of concentrated sulphuric acid, for 3 hours under reflux, with exclusion of moisture. The product is concentrated to half its volume and partitioned between methylene chloride and water. The organic phase is washed until neutral, dried with sodium sulphate and evaporated in vacuo to give 4-[4-(1-adamantyl)-phenoxy]-butyric acid ethyl ester of melting point 45°-46° C.
後処理
- temperatureunder reflux, with exclusion of moisture