反応式
[CH2:1]([NH2:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.[C:16](Cl)(=[O:18])[CH3:17].CO>C(Cl)Cl>[C:16]([NH:8][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)(=[O:18])[CH3:17]参加物
6
実験手順
10 g of benzylamine was dissolved in 200 ml of methylene chloride followed by the addition of 26 ml of triethylamine and dropwise addition of 7.3 ml of acetyl chloride at 0° C. After stirring for 1 hour at room temperature, 2 ml of methanol was added to the reaction system at 0° C. followed by 120 ml of water and separation of the phases. The aqueous layer was extracted with 100 ml of chloroform, and the resulting organic layer was concentrated after drying with anhydrous sodium sulfate to obtain 8.55 g of the target compound (yield: 61%).
後処理
- customfollowed by 120 ml of water and separation of the phases
- extractionThe aqueous layer was extracted with 100 ml of chloroform
- concentrationthe resulting organic layer was concentrated
- dry with materialafter drying with anhydrous sodium sulfate
出典と根拠
- ORDレコード
- ord-9f8371a37d84470292733eecc32aa446
- 出典データセット
- uspto-grants-2001_11
- 特許番号
- US06323212B1
関連ノート
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