反応式
[C:1]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)(=[O:5])[CH:2]([CH3:4])[CH3:3].S(Cl)([Cl:15])(=O)=O>CCCCCCC>[Cl:15][C:2]([CH3:4])([CH3:3])[C:1]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[O:5]参加物
4
実験手順
Isobutyrophenone (30.0 g, 0.20 mole) was dissolved in heptane (10 ml) and sulfuryl chloride (35 g, 0.26 mole) was added at once. After a few minutes gas evolution occurred. After 3 h of stirring at room temperature the reaction mixture was concentrated. The concentrate was dissolved in heptane (250 ml) and washed with 150 ml of an aqueous 2 wt % sodium bicarbonate solution. After drying over magnesium sulfate the solvent was removed under reduced pressure. The yield of 2-chloro-2-methylpropiophenone was 36.4 g or 98%.
後処理
- waitAfter a few minutes gas evolution occurred
- concentrationwas concentrated
- dissolutionThe concentrate was dissolved in heptane (250 ml)
- washwashed with 150 ml of an aqueous 2 wt % sodium bicarbonate solution
- dry with materialAfter drying over magnesium sulfate the solvent
- customwas removed under reduced pressure
出典と根拠
- ORDレコード
- ord-a07e5f5e6b3a40f2bc70bf1e69f1195a
- 出典データセット
- uspto-grants-2003_04
- 特許番号
- US06548710B2
関連ノート
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