反応式
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH2:6][CH2:7][CH2:8][C:9]2=O)([O-:3])=[O:2].C(O)C.Cl.[NH2:19][OH:20]>O>[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH2:6][CH2:7][CH2:8][C:9]2=[N:19][OH:20])([O-:3])=[O:2]参加物
5
実験手順
In a 100 mL flask equipped with a reflux condenser were placed 2.26 g of 5-nitro-1-tetralone and 60 mL of ethanol. To the mixture was added a solution of hydroxylamine hydrochloride (1.82 g) in water (4.5 mL). The content of the flask was stirred with a stirring bar at reflux for 8 hours. After evaporating the solvent, the residue was purified by column chromatography (eluent: hexane/ethyl acetate=5/1)′ to give 2.2 g of 5-nitro-1-tetralone oxime.
後処理
- customIn a 100 mL flask equipped with a reflux condenser
- temperatureat reflux for 8 hours
- customAfter evaporating the solvent
- customthe residue was purified by column chromatography (eluent: hexane/ethyl acetate=5/1)′
出典と根拠
- ORDレコード
- ord-8b6e3766710e4df5bfa902d7d9ed712c
- 出典データセット
- uspto-grants-2004_05
- 特許番号
- US06737548B2
関連ノート
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