反応式
[Cl:1][CH:2]=[CH:3][CH2:4][NH:5][CH2:6][CH2:7][O:8][CH3:9].C(N(CC)CC)C.[Cl:17][C:18]([Cl:23])([Cl:22])[C:19](Cl)=[O:20]>ClCCl>[Cl:1][CH:2]=[CH:3][CH2:4][N:5]([CH2:6][CH2:7][O:8][CH3:9])[C:19](=[O:20])[C:18]([Cl:23])([Cl:22])[Cl:17]参加物
5
実験手順
N-(3-chloro)allyl-N-methoxyethylamine (2.25 g, 0.015 mol) and 1.52 g (0.015 mol) triethylamine were stirred in 70 ml dichloromethane. The reaction was kept at approximately 5° C. with an ice-water bath. Trichloroacetyl chloride (2.73 g, 0.015 mol) in 10 ml dichloromethane was added dropwise to the cooled solution. Upon completion of the addition, the mixture was stirred at room temperature for 6 hours. The reaction mixture was then washed twice with saturated brine and dried with sodium sulfate. Rotary evaporation yielded 4.1 g of the above-named product.
後処理
- customThe reaction was kept at approximately 5° C. with an ice-water bath
- additionUpon completion of the addition
- washThe reaction mixture was then washed twice with saturated brine
- dry with materialdried with sodium sulfate
- customRotary evaporation
出典と根拠
- ORDレコード
- ord-8acb45df98e14c3a9a8f3a881c597456
- 出典データセット
- uspto-grants-1988_08
- 特許番号
- US04762548
関連ノート
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