反応式
[Na].[C:2]([CH2:10][CH:11]=O)(=[O:9])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[Cl-].O[NH2:15].[OH-].[Na+]>C(O)C>[C:2]([CH2:10][C:11]#[N:15])(=[O:9])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1参加物
6
実験手順
To a solution of 10 g sodium salt of benzoylacetaldehyde (prepared according to the procedure of Example 1) and 10 g hydroxyamine chloride in 30 ml ethanol was added 20 ml 50% NaOH at 0-10° C. The mixture was then refluxed for 24 hrs, and concentrated to 2/3 volume. The brown solution was neutralized with the concentrated hydrochloric acid. The precipitate was collected by filtration, and dried under vacuum to get a solid with slight pink color, 3.8 g benzoylacetonitrile.
後処理
- temperatureThe mixture was then refluxed for 24 hrs
- concentrationconcentrated to 2/3 volume
- filtrationThe precipitate was collected by filtration
- customdried under vacuum
出典と根拠
- ORDレコード
- ord-cfbda015927d4fc3aa2f4ef70d7d500d
- 出典データセット
- uspto-grants-2005_03
- 特許番号
- US06861162B2
関連ノート
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