反応式
[N:1]1[C:2](=[O:10])[CH:3]=[C:4]2[C:9]=1[CH:8]=[CH:7][CH:6]=[CH:5]2.Br[C:12]1[CH:20]=[C:19]2[C:15]([C:16](=O)[C:17](=[O:21])[NH:18]2)=[CH:14][CH:13]=1.Cl>C(O)(=O)C>[CH:13]1[CH:12]=[CH:20][C:19]2[NH:18][C:17](=[O:21])/[C:16](=[C:3]3\[C:4]4[CH:5]=[CH:6][CH:7]=[CH:8][C:9]=4[NH:1][C:2]\3=[O:10])/[C:15]=2[CH:14]=1参加物
5
実験手順
Separately adding 6-brome indolone (500 mg, 2.36 mmol), 6-bromoisatin (533 mg, 2.36 mmol of isatin), 15 mL glacial acetic acid and 0.1 mL HCl into a flask, heating and refluxing for 24 hours. Stop the reaction and cooling to room temperature, filtering to obtain a solid, and then washing the solid by water, ethanol, and ethyl acetate. Drying the final product in a vacuum drying box, get brown 6,6′-bidromo isoindigo, the yield was 95%.
後処理
- temperatureheating
- temperaturerefluxing for 24 hours
- customthe reaction
- filtrationfiltering
- customto obtain a solid
- washwashing the solid by water, ethanol, and ethyl acetate
- dry with materialDrying the final product in a vacuum
- customdrying box
出典と根拠
- ORDレコード
- ord-33af6b66062c439f94a228dd305491d4
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08889825B2
関連ノート
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