反応式
CN[N+]([O-])=O.S(=O)(=O)(O)O.[NH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.CN([N+]([O-])=O)[C:20]1[C:25]([N+]([O-])=O)=[CH:24][C:23]([N+]([O-])=O)=[CH:22][C:21]=1[N+]([O-])=O>>[C:12]1([NH:11][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1参加物
5
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-baebf6613e4c4de5988b6c60858d0ccb
- 出典データセット
- uspto-grants-1985_04
- 特許番号
- US04513148
関連ノート
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