反応式
[CH:1](=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[NH2:10][OH:11]>CO.O>[CH:1](=[N:10][OH:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
実験手順
10.0 mmol of Benzaldehyde was dissolved in 30 ml of 30% solution of CH3OH and H2O, and added into a triangular flask equipped with magnetic stirrer. 10.0 mmol of hydroxylamine hydrochloride was added under stirring. After hydroxylamine hydrochloride was dissolved, 5.0 mmol of dry and porphyrized sodium carbonate was slowly added. The reaction was carried out at room temperature. After the completion of the reaction monitored by TLC, methanol was removed from the system under reduced pressure. 30 ml H2O and dichloromethane (3×30 ml) were added to extract the mixture. The organic layers were combined, and then dried over anhydrous sodium sulfate. The solvent was removed to afford a crude product of benzaldehyde oxime in 86.2% yield. The crude material was directly used in the next reaction without separation and purification.
後処理
- additionadded into a triangular flask
- customequipped with magnetic stirrer
- custom5.0 mmol of dry
- additionporphyrized sodium carbonate was slowly added
- customwas carried out at room temperature
- customwas removed from the system under reduced pressure
- addition30 ml H2O and dichloromethane (3×30 ml) were added
- extractionto extract the mixture
- dry with materialdried over anhydrous sodium sulfate
- customThe solvent was removed
出典と根拠
- ORDレコード
- ord-89dd62ee9ec24867853d6697c9d91541
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09434741B2
関連ノート
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