Thionyl Chloride → 2-(4-Chlorophenyl)-2-methylpropanoyl chloride
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:13])([CH3:12])[C:9](O)=[O:10])=[CH:4][CH:3]=1.S(Cl)([Cl:16])=O>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:13])([CH3:12])[C:9]([Cl:16])=[O:10])=[CH:4][CH:3]=1参加物
4
実験手順
2-(4-Chlorophenyl)-2-methylpropanoic acid (3.85 g, 19.4 mmol) in toluene (5 mL) and thionyl chloride (5.00 g, 3.1 mL) was heated at 80° C. for 2 hours. The mixture was cooled and concentrated under reduced pressure to provide the title compound.
後処理
- temperatureThe mixture was cooled
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-e1369f3beefb40839e681d647c5c4b1a
- 出典データセット
- uspto-grants-2005_08
- 特許番号
- US06933311B2
反応ノート
読み込み中…