Nitric Acid → 1,3,5-Trimethyl-4-nitro-1H-pyrazole
反応式
N1C=C[CH:3]=N1.[N:6]1[CH:11]=CC=[CH:8][C:7]=1[CH2:12][C:13]1[NH:17]N=NN=1.[N+:18]([O-:21])(O)=[O:19]>S(=O)(=O)(O)O>[N+:18]([C:12]1[C:13]([CH3:3])=[N:17][N:6]([CH3:11])[C:7]=1[CH3:8])([O-:21])=[O:19]参加物
5
反応条件
- 温度
- 0 °C
実験手順
The pyrazole from (a) above (3.1 g; 0.028, moles) was dissolved in cold sulfuric acid (15 mL), cooled to 0° C., and then treated with fuming nitric acid (12 mL). The acidic solution was heated on a steam bath for 2 hours, cooled to room temperature, and poured over ice. The solution was made basic (pH=12) and the precipitate was collected by filtration and washed with water. Yield: 2.3 g (53%), white solid.
後処理
- temperatureThe acidic solution was heated on a steam bath for 2 hours
- temperaturecooled to room temperature
- additionpoured over ice
- filtrationthe precipitate was collected by filtration
- washwashed with water
出典と根拠
- ORDレコード
- ord-ee2a840ed95c4d11bbc058a0d206d5f5
- 出典データセット
- uspto-grants-1995_08
- 特許番号
- US05441975
反応ノート
読み込み中…