反応式
Cl.[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][NH2:10])=[CH:5][CH:4]=1.C(N([CH2:16][CH3:17])CC)C.[OH2:18]>>[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][NH:10][C:16](=[O:18])[CH3:17])=[CH:5][CH:4]=1参加物
4
反応条件
- 温度
- 0 °C
実験手順
12.5 g of 4-chlorophenylhydrazine hydrochloride are dissolved in 100 ml of water and then triethylamine is added until the salt has been neutralized. Extraction is carried out with AcOEt and then the extract is evaporated to dryness. The base is dissolved in 100 ml of ether, the solution is cooled to 0° C. and then 15 ml of acetic anhydride are added dropwise. The mixture is stirred at 0° C. for 15 minutes. The white precipitate formed is filtered off and is then washed with ether to produce 12.8 g of the expected compound in the form of a white powder.
後処理
- extractionExtraction
- customthe extract is evaporated to dryness
- dissolutionThe base is dissolved in 100 ml of ether
- addition15 ml of acetic anhydride are added dropwise
- customThe white precipitate formed
- filtrationis filtered off
- washis then washed with ether
出典と根拠
- ORDレコード
- ord-f8e7896bab57401bbf915fd5deba8d5f
- 出典データセット
- uspto-grants-2011_09
- 特許番号
- US08012991B2
関連ノート
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