Thionyl Chloride → (2-Chloro-4-methoxyphenyl)acetyl chloride
反応式
[Cl:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[CH:4][C:3]=1[CH2:10][C:11]([OH:13])=O.S(Cl)([Cl:16])=O>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[CH:4][C:3]=1[CH2:10][C:11]([Cl:16])=[O:13]参加物
4
実験手順
160 g of 2-chloro-4-methoxyphenylacetic acid are suspended in 210 ml of toluene, and the suspension is stirred together with 96 ml of thionyl chloride at 80° C. until the evolution of gas has ceased. The volatile components are stripped off, and the residue is distilled. 90 g of an orange oil are obtained (thin-film evaporator 170° C., 0.08 mbar).
後処理
- distillationthe residue is distilled
出典と根拠
- ORDレコード
- ord-24d808e8b3a94d99a0479958d73eed3d
- 出典データセット
- uspto-grants-2005_09
- 特許番号
- US06939888B2
反応ノート
読み込み中…