反応式
[F:1][C:2]1[CH:16]=[CH:15][C:5]([C:6]([C:8]2[CH:13]=[CH:12][N+:11]([O-])=[CH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1.O=P(Cl)(Cl)[Cl:19]>>[Cl:19][C:12]1[CH:13]=[C:8]([C:6](=[O:7])[C:5]2[CH:15]=[CH:16][C:2]([F:1])=[CH:3][CH:4]=2)[CH:9]=[CH:10][N:11]=1参加物
3
実験手順
0.88 g 4-(4-fluorobenzoyl)-pyridine N-oxide and 50 ml POCl3 are refluxed for 2 hrs. Excess POCl3 is distilled at normal pressure. The crude is treated with slightly alkaline cold water and then extracted with methylene chloride. Working as usual affords 0.80 g of title product, identical with that obtained by the Friedel-Crafts process (see Ex. 3d).
後処理
- distillationExcess POCl3 is distilled at normal pressure
- additionThe crude is treated with slightly alkaline cold water
- extractionextracted with methylene chloride
出典と根拠
- ORDレコード
- ord-297ae98322534e3db5a0a6253499a89f
- 出典データセット
- uspto-grants-1988_04
- 特許番号
- US04736037
関連ノート
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