Ammonia → Allyl 4-allyloxy-3-aminobenzoate
反応式
[CH2:1]([O:4][C:5]1[CH:16]=[CH:15][C:8]([C:9]([O:11][CH2:12][CH:13]=[CH2:14])=[O:10])=[CH:7][C:6]=1[N+:17]([O-])=O)[CH:2]=[CH2:3].C(OC1C=C([N+]([O-])=O)C=CC=1C(OCC=C)=O)C=C.N>CO>[CH2:1]([O:4][C:5]1[CH:16]=[CH:15][C:8]([C:9]([O:11][CH2:12][CH:13]=[CH2:14])=[O:10])=[CH:7][C:6]=1[NH2:17])[CH:2]=[CH2:3]参加物
5
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 that the solvent was methanol, and using an aqueous solution of ammonia in place of sodium bicarbonate in the work-up, to give allyl 4-allyloxy-3-aminobenzoate.
出典と根拠
- ORDレコード
- ord-4b065fbabcf24293b417dcacb350f0a1
- 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…