反応式
[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)(=[O:4])=[O:3].[N+:11]([O-])([OH:13])=[O:12].C(=O)(O)[O-].[Na+]>>[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([N+:11]([O-:13])=[O:12])[CH:6]=1)(=[O:4])=[O:3]参加物
4
実験手順
Phenyl methyl sulphone (4.0 g) was added, portionwise, to fuming nitric acid stirred at 0° C. The reaction mixture was allowed to warm to room temperature, stirred for 1 hour, and then poured carefully onto ice. The solution was carefully neutralised with sodium bicarbonate and the mixture filtered at the pump. The solid collected was washed with water and dried under reduced pressure over potassium hydroxide to give the title compound as a white solid (5.63 g) in a sufficient state of purity for the next reaction.
後処理
- additionpoured carefully onto ice
- filtrationthe mixture filtered at the pump
- customThe solid collected
- washwas washed with water
- dry with materialdried under reduced pressure over potassium hydroxide
出典と根拠
- ORDレコード
- ord-4f46a697ee1449fb83383b349f6ca7b4
- 出典データセット
- uspto-grants-1999_01
- 特許番号
- US05856273
関連ノート
読み込み中…