反応式
[C:1]1([CH3:10])[CH:6]=[CH:5][CH:4]=[C:3]([C:7](=[O:9])[CH3:8])[CH:2]=1.[Br:11]Br.CCOCC>O1CCOCC1>[Br:11][CH2:8][C:7]([C:3]1[CH:2]=[C:1]([CH3:10])[CH:6]=[CH:5][CH:4]=1)=[O:9]参加物
5
実験手順
To a solution of 1-m-tolyl-ethanone (6.0 g, 44.72 mmol) in dioxane (5 ml), bromine (7.14 g, 44.72 mmol) in dioxane (10 ml) and ether (15 ml) was added and stirred at room temperature for 5 hr. The reaction mixture was poured into ice water and the compound was extracted using ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate, filtered and then evaporated to give crude 2-bromo-1-m-tolyl-ethanone, 7.6 g (80%). The crude compound obtained was used in the next step without further purification.
後処理
- extractionthe compound was extracted
- washThe organic layer was washed with water and brine
- dry with materialdried over anhydrous sodium sulfate
- filtrationfiltered
- customevaporated
- customto give crude 2-bromo-1-m-tolyl-ethanone, 7.6 g (80%)
出典と根拠
- ORDレコード
- ord-0586c48dda1c4b35beae4608fb38fbc0
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08486962B2
関連ノート
読み込み中…