Ammonia → Diallyl 2-aminobenzene-1,4-dicarboxylate
反応式
[N+:1]([C:4]1[CH:9]=[C:8]([C:10]([O:12][CH2:13][CH:14]=[CH2:15])=[O:11])[CH:7]=[CH:6][C:5]=1[C:16]([O:18][CH2:19][CH:20]=[CH2:21])=[O:17])([O-])=O.C(OC1C=C([N+]([O-])=O)C=CC=1C(OCC=C)=O)C=C.N>>[NH2:1][C:4]1[CH:9]=[C:8]([C:10]([O:12][CH2:13][CH:14]=[CH2:15])=[O:11])[CH:7]=[CH:6][C:5]=1[C:16]([O:18][CH2:19][CH:20]=[CH2:21])=[O:17]参加物
4
実験手順
The above nitro compound was reduced by the method described in example 1, for the reduction of allyl 2-allyloxy-4-nitrobenzoate, except using an aqueous solution of ammonia in place of sodium bicarbonate in the work-up, to give diallyl 2-aminobenzene-1,4-dicarboxylate.
出典と根拠
- ORDレコード
- ord-1bd6b853c3ed48ac8fbec647d45a4af5
- 出典データセット
- uspto-grants-1996_07
- 特許番号
- US05541178
反応ノート
読み込み中…