反応式
[Br:1][C:2]1[CH:3]=[C:4]([C:8](=[O:10])[CH3:9])[CH:5]=[CH:6][CH:7]=1.[Br:11]Br>C(O)(=O)C>[Br:11][CH2:9][C:8]([C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([Br:1])[CH:3]=1)=[O:10]参加物
4
反応条件
- 温度
- 60 °C
実験手順
Into a 500-mL 3-necked round-bottom flask, was placed a solution of 1-(3-bromophenyl)ethanone (40 g, 202.02 mmol, 1.00 equiv) in acetic acid (200 mL). This was followed by the addition of a solution of Br2 (32 g, 200.00 mmol) in acetic acid (50 mL) dropwise with stirring at 60° C. The resulting solution was stirred for 3 h at 60° C. in an oil bath. The resulting mixture was concentrated under vacuum. The crude product was re-crystallized from petroleum ether:ethyl acetate in the ratio of 8:1. This resulted in 24 g (43%) of 2-bromo-1-(3-bromophenyl)ethanone as a yellow solid.
後処理
- customInto a 500-mL 3-necked round-bottom flask, was placed
- stirringThe resulting solution was stirred for 3 h at 60° C. in an oil bath
- concentrationThe resulting mixture was concentrated under vacuum
- customThe crude product was re-crystallized from petroleum ether
- customThis resulted in 24 g (43%) of 2-bromo-1-(3-bromophenyl)ethanone as a yellow solid
出典と根拠
- ORDレコード
- ord-543de9c65f6e42f7ac21c2a1f2b683ee
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08541448B2
関連ノート
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