反応式
[CH3:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][NH:5][C:4](=[O:11])[CH:3]=1.[Br:12]Br>O>[Br:12][C:3]1[C:4](=[O:11])[NH:5][CH:6]=[C:7]([N+:8]([O-:10])=[O:9])[C:2]=1[CH3:1]参加物
4
反応条件
- 温度
- 10 °C
実験手順
In a 1000 ml three-necked round-bottomed flask, 5.00 g of 4-methyl-5-nitro-1H-pyridin-2-one (CA registry number: 21901-41-7) is suspended in 500 ml of water. Under stirring, the mixture is kept at a temperature of 40° C. while 1.83 ml of elemental bromine is added dropwise. Stirring at 40° C. is continued for an additional 4 hours. Afterwards, the mixture is cooled to 10° C. and the resulting precipitate collected by filtration and washed with water (4×). After drying, 6.65 g of the title compound is obtained in the form of a beige solid (MP: 237-240° C.).
後処理
- additionis added dropwise
- stirringStirring at 40° C.
- filtrationthe resulting precipitate collected by filtration
- washwashed with water (4×)
- customAfter drying
出典と根拠
- ORDレコード
- ord-060f95c1ea164b63ae0bb07e83e11221
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09096525B2
関連ノート
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