反応式
[Br:1][C:2]1[C:3]([CH3:12])=[CH:4][C:5]([CH3:11])=[C:6]([CH:10]=1)[C:7]([OH:9])=[O:8].OS(O)(=O)=O.[N+:18]([O-])([OH:20])=[O:19]>>[Br:1][C:2]1[C:3]([CH3:12])=[C:4]([N+:18]([O-:20])=[O:19])[C:5]([CH3:11])=[C:6]([CH:10]=1)[C:7]([OH:9])=[O:8]参加物
4
反応条件
- 温度
- -10 °C
実験手順
5-Bromo-2,4-dimethylbenzoic acid (12 g, 52.17 mmol) was added to cooled conc. H2SO4 (48 mL) at −10° C. lot wise. After 10 minutes nitrating mixture {prepared as mixing Conc. HNO3 (6 mL) with conc.H2SO4 (24 mL)} was added drop wise at −10° C. Resulting reaction mass was stirred at −10° C. for 30 minutes. On completion, reaction mixture was poured on ice cold water, solid precipitated was filtered, washed with water and dried under vacuum giving desired compound (13 g, 91%).
後処理
- custommixture {prepared
- customResulting
- customreaction mass
- customOn completion, reaction mixture
- additionwas poured on ice cold water, solid
- customprecipitated
- filtrationwas filtered
- washwashed with water
- customdried under vacuum
出典と根拠
- ORDレコード
- ord-605d50c7682244c88c1ca871eeafdb64
- 出典データセット
- uspto-grants-2016_06
- 特許番号
- US09376422B2
関連ノート
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