Hydrazine → Hydrazine hydrate (1:1)
反応式
C[O:2]C1C=C(NC(=O)C)C([N+]([O-])=O)=CC=1C(OC)=O.[CH3:20][O:21][C:22]1[CH:30]=[C:29]([NH2:31])[C:28]([N+:32]([O-])=O)=[CH:27][C:23]=1[C:24]([O-:26])=[O:25].[Na+].[NH2:36][NH2:37]>>[OH2:2].[NH2:36][NH2:37].[CH3:20][O:21][C:22]1[CH:30]=[C:29]([NH2:31])[C:28]([NH2:32])=[CH:27][C:23]=1[C:24]([OH:26])=[O:25]参加物
5
実験手順
In general, reaction of methyl 2-methoxy-4-acetylamino-5-nitrobenzoate with the base is preferably immediately followed by the in-situ reaction of the intermediate sodium-2-methoxy- 4-amino-5-nitrobenzoate (intermediate I) with hydrazine or its equivalent, preferably as hydrazine hydrate, to form 2-methoxy-4,5-diaminobenzoic acid (intermediate II). That product is preferably recovered and purified prior to further use.
出典と根拠
- ORDレコード
- ord-c6ea9cca305d4b5792bf9487e008496f
- 出典データセット
- uspto-grants-1989_02
- 特許番号
- US04804765
反応ノート
読み込み中…