HCID 14208511、化合物 → 1-Methoxy-4-nitro-3-(2-nitroethenyl)-2-(phenylmethoxy)benzene
反応式
[CH2:1]([O:8][C:9]1[C:16]([O:17][CH2:18]C)=[CH:15][CH:14]=[C:13]([N+:20]([O-:22])=[O:21])[C:10]=1[CH:11]=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(OC1C(OC)=CC=[C:35]([N+:41]([O-:43])=[O:42])C=1C=O)C1C=CC=CC=1>>[CH2:1]([O:8][C:9]1[C:16]([O:17][CH3:18])=[CH:15][CH:14]=[C:13]([N+:20]([O-:22])=[O:21])[C:10]=1[CH:11]=[CH:35][N+:41]([O-:43])=[O:42])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
3
実験手順
This compound is obtained according to the operating method described in Example 1b, in which the 2-benzyloxy-3-ethoxy-6-nitrobenzaldehyde is replaced with 2-benzyloxy-3-methoxy-6-nitrobenzaldehyde. A pale yellow powder (yield=83%, m.p.=118°-119° C.) is obtained.
後処理
- customThis compound is obtained
出典と根拠
- ORDレコード
- ord-ced1cf81adcb4b8e869d5692bde581ef
- 出典データセット
- uspto-grants-1992_07
- 特許番号
- US05131911
反応ノート
読み込み中…