Nitric Acid → 5-Bromo-2-methoxy-3-nitrobenzaldehyde
反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][CH3:11])=[C:6]([CH:9]=1)[CH:7]=[O:8].[N+:12]([O-])([OH:14])=[O:13]>S(=O)(=O)(O)O>[Br:1][C:2]1[CH:3]=[C:4]([N+:12]([O-:14])=[O:13])[C:5]([O:10][CH3:11])=[C:6]([CH:9]=1)[CH:7]=[O:8]参加物
4
実験手順
5-Bromo-2-methoxybenzaldehyde (29.65 g, 138 mmol) was added to stirred concentrated sulfuric acid (160 mL) at −15° C. Nitric acid (70% w/w) (16 g) was added dropwise. Further stirring was allowed for 15 mins at this temperature before the mixture was poured onto crushed ice (2 L). The resulting precipitate was collected by filtration and partitioned between dichloromethane (800 mL) and saturated sodium hydrogen carbonate (1 L). The organic layer was dried (Na2SO4) and evaporated in vacuo to give the title compound (20.5 g) as a crude solid.
後処理
- additionwas poured
- filtrationThe resulting precipitate was collected by filtration
- custompartitioned between dichloromethane (800 mL) and saturated sodium hydrogen carbonate (1 L)
- dry with materialThe organic layer was dried (Na2SO4)
- customevaporated in vacuo
出典と根拠
- ORDレコード
- ord-bf32651281b14c6ebabefb440b72bb2d
- 出典データセット
- uspto-grants-2007_05
- 特許番号
- US07214674B2
反応ノート
読み込み中…