反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:12][C:11]([C:13](=[O:15])[CH3:14])=[CH:10][CH:9]=2)=[CH:4][CH:3]=1.[Cl:16][C:17]1[C:24]([Cl:25])=[C:23]([OH:26])[CH:22]=[CH:21][C:18]=1[CH:19]=O>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:12][C:11]([C:13](=[O:15])[CH:14]=[CH:19][C:18]3[CH:21]=[CH:22][C:23]([OH:26])=[C:24]([Cl:25])[C:17]=3[Cl:16])=[CH:10][CH:9]=2)=[CH:4][CH:3]=1参加物
3
実験手順
1-(5-(4-Bromophenyl)thien-2-yl)-3-(2,3-dichloro-4-hydroxyphenyl)prop-2-en-1-one is prepared from 1-(5-(4-bromophenyl)thien-2-yl)ethanone and 2,3-dichloro-4-hydroxybenzaldehyde according to general procedure B. The evaporation residue is washed with dichloromethane.
後処理
- washThe evaporation residue is washed with dichloromethane
出典と根拠
- ORDレコード
- ord-99ab30ca15c64a4196374ccdb51f0af3
- 出典データセット
- uspto-grants-2012_01
- 特許番号
- US08088819B2
関連ノート
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