反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[F:10])[C:5]#N.[OH2:11]>[Ni].C(O)=O>[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[F:10])[CH:5]=[O:11]参加物
5
実験手順
17.0 g of a 50% strength alkaline suspension of Raney nickel were filtered under a nitrogen atmosphere and the material on the filter was washed until neutral. The Raney nickel obtained by this method was suspended in 150 ml of formic acid. 20.0 g (0.1 mole) of 3-bromo-4-fluoro-benzonitrile were added to this suspension. The mixture was heated at 80° to 90° C. for 3 to 5 hours and the reaction mixture was then cooled and poured into 300 ml of water. After filtering, the filtrate was twice extracted with, in each case, 200 ml of toluene. The toluene phase was dried over sodium sulphate and then concentrated. 17.2 g (85% of theory) of 3-bromo-4-fluoro-benzaldehyde with a boiling point of 63°-65° C./0.3 mm Hg were obtained.
後処理
- filtrationwere filtered under a nitrogen atmosphere
- washthe material on the filter was washed until neutral
- customThe Raney nickel obtained by this method
- temperatureThe mixture was heated at 80° to 90° C. for 3 to 5 hours
- temperaturethe reaction mixture was then cooled
- filtrationAfter filtering
- extractionthe filtrate was twice extracted with, in each case, 200 ml of toluene
- dry with materialThe toluene phase was dried over sodium sulphate
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-a7d4e6788f22427e80515f37aff1301f
- 出典データセット
- uspto-grants-1983_05
- 特許番号
- US04383949
関連ノート
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