3-Nitro-2-phenylthiophene → 2-Phenylthiophen-3-amine
反応式
[N+:1]([C:4]1[CH:8]=[CH:7][S:6][C:5]=1[C:9]1[CH:14]=[CH:13][C:12](Cl)=[CH:11][CH:10]=1)([O-])=O.[N+](C1C=CSC=1C1C=CC=CC=1)([O-])=O>>[NH2:1][C:4]1[CH:8]=[CH:7][S:6][C:5]=1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1参加物
3
実験手順
The same procedures as described in Example 3 were carried out except that 3-nitro-2-(4-chlorophenyl)thiophene was replaced by 3-nitro-2-phenylthiophene. The yield was 81%. 1H-NMR(CDCl3, δ value):3.82(2H, brs), 6.66(1H, d, J=5.1), 7.12(1H, d, J=5.1), 7.22-7.29(1H, m), 7.42(2H, dt, J=1.5, 7.3), 7.52(2H, dd, J=1.5, 7.3)
出典と根拠
- ORDレコード
- ord-76c78543a953450d946f163bb0b939a2
- 出典データセット
- uspto-grants-1998_05
- 特許番号
- US05747518
反応ノート
読み込み中…