反応式
[CH3:1][NH:2][N+:3]([O-:5])=[O:4].[C:6]1(Cl)[C:7](=[CH:11][C:12](=[CH:16][C:17]=1[N+:18]([O-:20])=[O:19])[N+:13]([O-:15])=[O:14])[N+:8]([O-:10])=[O:9]>>[CH3:1][N:2]([N+:3]([O-:5])=[O:4])[C:11]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][C:17]([N+:18]([O-:20])=[O:19])=[CH:16][C:12]=1[N+:13]([O-:15])=[O:14]参加物
3
実験手順
Methylnitramine decomposes explosively in contact with concentrated sulfuric acid. It is evolved when aniline reacts with tetryl; a diphenylamine derivative is produced simultaneously. Methylnitramine reacts with picryl chloride to form tetryl.
出典と根拠
- ORDレコード
- ord-4b5c3c106cac439bb2893829271ee286
- 出典データセット
- uspto-grants-1985_04
- 特許番号
- US04513148
関連ノート
読み込み中…