3,5-Dibromo-4-Hydroxybenzaldehyde → 1-[2-Hydroxy-4-carboxydimethylmethyloxyphenyl]-3-[3,5-dibromo-4-hydroxyphenyl]prop-2-en-1-one
反応式
[OH:1][C:2]1[C:7]([O:8][CH3:9])=[C:6]([C:10]([O:12]CC)=[O:11])[C:5]([CH3:15])=[C:4]([CH3:16])[C:3]=1[C:17](=[O:35])[CH:18]=CC1C=C(C(C)(C)C)C(O)=C(C(C)(C)C)C=1.[Br:36][C:37]1[CH:38]=[C:39]([CH:42]=[C:43]([Br:46])[C:44]=1[OH:45])[CH:40]=O>>[OH:1][C:2]1[C:7]([O:8][CH3:9])=[C:6]([C:10]([OH:12])=[O:11])[C:5]([CH3:15])=[C:4]([CH3:16])[C:3]=1[C:17](=[O:35])[CH:18]=[CH:40][C:39]1[CH:38]=[C:37]([Br:36])[C:44]([OH:45])=[C:43]([Br:46])[CH:42]=1参加物
3
実験手順
This compound was synthesized from 2′-hydroxy-4′-(ethoxycarbonyldimethylmethyloxy)acetophenone (starting material 1) and 3,5-dibromo-4-hydroxybenzaldehyde according to general method 2 described earlier.
出典と根拠
- ORDレコード
- ord-52c82fb47f91453c9126b8ff89d7cd96