反応式
[Br:1]Br.[C:3]([C:6]1[CH:7]=[C:8]([CH:11]=[CH:12][CH:13]=1)[C:9]#[N:10])(=[O:5])[CH3:4].O>CCOCC>[Br:1][CH2:4][C:3]([C:6]1[CH:7]=[C:8]([CH:11]=[CH:12][CH:13]=1)[C:9]#[N:10])=[O:5]参加物
5
実験手順
Br2 (1 mmol) was dropwise added to a solution of 3-acetylbenzonitrile (1 mmol) in Et2O (15 ml) at 0° C., and then the mixture was stirred at r.t. for 4 h. Water was added, and the mixture was extracted with EtOAc. The organic layer was dried over Na2SO4, and was concentrated to give an oil, i.e., 3-(2-bromoacetyl)benzonitrile, which was directly used for the next step without purification.
後処理
- extractionthe mixture was extracted with EtOAc
- dry with materialThe organic layer was dried over Na2SO4
- concentrationwas concentrated
出典と根拠
- ORDレコード
- ord-bc195a55eb7041ccb0c4ce7b56ac6d09
- 出典データセット
- uspto-grants-2011_01
- 特許番号
- US07868001B2
関連ノート
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