Ethanol → Ethyl [4-(2-Bromoethyl)phenyl]acetate
反応式
[Br:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]([OH:13])=[O:12])=[CH:6][CH:5]=1.S(=O)(=O)(O)O.[CH2:19](O)[CH3:20]>>[Br:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]([O:13][CH2:19][CH3:20])=[O:12])=[CH:6][CH:5]=1参加物
4
実験手順
A solution of [4-(2-bromoethyl)phenyl]acetic acid (48.6 g., 0.2 mole) and sulfuric acid (1.5 ml.) in ethanol (400 ml.) is boiled under reflux for 6 hours. About 300 ml. of the ethanol is removed by distillation at reduced pressure. The residue is diluted with 400 ml. of water. The oily ester is taken up in ether, washed with water and brine, and dried over magnesium sulfate. Evaporation of the ether leaves the title compound as an oil which can be purified by distillation in vacuo.
後処理
- temperatureunder reflux for 6 hours
- customof the ethanol is removed by distillation at reduced pressure
- additionThe residue is diluted with 400 ml
- washwashed with water and brine
- dry with materialdried over magnesium sulfate
- customEvaporation of the ether
出典と根拠
- ORDレコード
- ord-1245073431ed4b0089641a70544a7e72
- 出典データセット
- uspto-grants-1979_04
- 特許番号
- US04150235
反応ノート
読み込み中…