Pyridine → 2-Fluoro-4-(propoxymethyl)benzoyl chloride
反応式
[F:1][C:2]1[CH:10]=[C:9]([CH2:11][O:12][CH2:13][CH2:14][CH3:15])[CH:8]=[CH:7][C:3]=1[C:4](O)=[O:5].S(Cl)([Cl:18])=O.N1C=CC=CC=1>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:10]=[C:9]([CH2:11][O:12][CH2:13][CH2:14][CH3:15])[CH:8]=[CH:7][C:3]=1[C:4]([Cl:18])=[O:5]参加物
5
実験手順
2-Fluoro-4-(propoxymethyl)benzoic acid (1.5 g, 7.1 mmol) was mixed with thionyl chloride (1.3 g, 10.6 mmol), pyridine (0.1 ml) and toluene (3 ml), followed by reacting them at 80° C. for 2 hours, and distilling off superfluous thionyl chloride and toluene under reduced pressure, to obtain raw 2-fluoro-4-(propoxymethyl)benzoyl chloride.
後処理
- customat 80° C.
- customfor 2 hours
- distillationdistilling off superfluous thionyl chloride and toluene under reduced pressure
出典と根拠
- ORDレコード
- ord-76b1df71253240668446a661b9803ec5
- 出典データセット
- uspto-grants-1998_05
- 特許番号
- US05755994
反応ノート
読み込み中…