反応式
[CH:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:7](Cl)(=[O:10])[CH:8]=[CH2:9].[Cl-].[Al+3].[Cl-].[Cl-].Cl>ClCCl>[C:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)(=[O:10])[CH:8]=[CH2:9]参加物
6
反応条件
- 温度
- 0 °C
実験手順
Benzene (1 mL), acryloyl chloride (0.4 mL), and aluminium chloride (0.33 g) were added to dichloromethane (4 mL), followed by stirring at 0° C. for 2 hours. After reaction, 1 N hydrochloric acid and dichlormethane (5 mL) were added in order. The organic phase was concentrated. The obtained residue was applied to a silica gel column to obtain the title compound (120 mg).
後処理
- additionwere added in order
- concentrationThe organic phase was concentrated
出典と根拠
- ORDレコード
- ord-705956e2f9754b308b883e365c03e0ab
- 出典データセット
- uspto-grants-2015_01
- 特許番号
- US08937091B2
関連ノート
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