Nitrilooxonium tetrafluoroborate → 7-Fluoro-2-nitronaphthalene
反応式
[N+:1]([C:4]1[CH:13]=[C:12]2[C:7]([CH:8]=[CH:9][C:10](N)=[CH:11]2)=[CH:6][CH:5]=1)([O-:3])=[O:2].[F:15][B-](F)(F)F.N#[O+]>ClCCl>[F:15][C:10]1[CH:11]=[C:12]2[C:7]([CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:13]2)=[CH:8][CH:9]=1参加物
4
実験手順
A mixture 7-nitro-2-aminonaphthalene (1 g, 5.31 mmol) and nitrosonium tetrafluoroborate (931 mg, 7.97 mmol) in dichloromethane (10 mL) is stirred at room temperature for 12 hours and at 110° C. for 1 hour. After cooling to room temperature, the reaction mixture is concentrated by rotary evaporator under high vacuum. The residual oil is purified by flash chromatography on silica gel (3:1 hexanes/EtOAc) to give 7-fluoro-2-nitronaphthalene as a dark red solid.
後処理
- concentrationthe reaction mixture is concentrated by rotary evaporator under high vacuum
- customThe residual oil is purified by flash chromatography on silica gel (3:1 hexanes/EtOAc)
出典と根拠
- ORDレコード
- ord-00452f2f90c640288769d270a3a68b97
- 出典データセット
- uspto-grants-2007_04
- 特許番号
- US07202364B2
反応ノート
読み込み中…