反応式
Br[CH2:2][C:3]([C:5]1[CH:12]=[CH:11][C:8]([C:9]#[N:10])=[CH:7][CH:6]=1)=[O:4].[N-:13]=[N+:14]=[N-:15].[Na+]>CO>[N:13]([CH2:2][C:3]([C:5]1[CH:12]=[CH:11][C:8]([C:9]#[N:10])=[CH:7][CH:6]=1)=[O:4])=[N+:14]=[N-:15]参加物
4
実験手順
To a solution of the commercially available 4-bromoacetyl-benzonitrile (5 g, 22.32 mmol) in 150 mL of methanol was added sodium azide (1.74 g, 26.78 mmol) and the contents stirred at room temperature for 2 h. After removal of the solvent, the residue was treated with water (50 mL) and extracted with dichloromethane (3×50 mL). The combined organic layers were dried over MgSO4 and concentrated to give a yellow solid (3.90 g, 94%). This compound was used for the next step without any further purification.
後処理
- customAfter removal of the solvent
- additionthe residue was treated with water (50 mL)
- extractionextracted with dichloromethane (3×50 mL)
- dry with materialThe combined organic layers were dried over MgSO4
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-b2c5886bde8446999e9f1ed768a4f001
- 出典データセット
- uspto-grants-2014_02
- 特許番号
- US08658659B2
関連ノート
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