Ethanol → Benzeneacetic acid, 3,5-dibromo-4-hydroxy-, ethyl ester
反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH2:10][C:11]([OH:13])=[O:12])[CH:5]=[C:6]([Br:9])[C:7]=1[OH:8].S(=O)(=O)(O)O.[CH2:19](O)[CH3:20]>>[Br:1][C:2]1[CH:3]=[C:4]([CH2:10][C:11]([O:13][CH2:19][CH3:20])=[O:12])[CH:5]=[C:6]([Br:9])[C:7]=1[OH:8]参加物
4
実験手順
3,5-Dibromo-4-hydroxyphenylacetic acid (60 g, 0.19 mol), from Preparation A, was suspended in 1 L of ethanol and 10 mL of concentrated sulfuric acid and heated at reflux overnight. The reaction mixture was cooled, concentrated and the product collected by filtration, washed with water, and dried in a vacuum oven to obtain ethyl 3,5-dibromo-4-hydroxyphenylacetate.
後処理
- temperatureat reflux overnight
- temperatureThe reaction mixture was cooled
- concentrationconcentrated
- filtrationthe product collected by filtration
- washwashed with water
- customdried in a vacuum oven
出典と根拠
- ORDレコード
- ord-bddfa451827142e3b0ae96b43ddcd2e1
- 出典データセット
- uspto-grants-1994_02
- 特許番号
- US05284971
反応ノート
読み込み中…