6-Benzoylbenzoselenazolinone → Bis(2-amino-5-benzoylphenyl) diselenide
反応式
[C:1]([C:9]1[CH:18]=[CH:17][C:12]2[N:13]=C[Se:15](=O)[C:11]=2[CH:10]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>[OH-].[Na+]>[NH2:13][C:12]1[CH:17]=[CH:18][C:9]([C:1](=[O:8])[C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[CH:10][C:11]=1[Se:15][Se:15][C:11]1[CH:10]=[C:9]([C:1](=[O:8])[C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH:18]=[CH:17][C:12]=1[NH2:13]参加物
3
実験手順
1.5 g (0.005 mol) of 6-benzoylbenzoselenazolinone are introduced together with 20 cm3 of 10% sodium hydroxide into a ground-necked flask. The mixture is heated to reflux with stirring for two hours. After cooling, the reaction medium is neutralized. The precipitate is drained, washed with water and dried and the product is recrystallized in toluene.
後処理
- temperatureThe mixture is heated
- temperatureto reflux
- temperatureAfter cooling
- washwashed with water
- customdried
- customthe product is recrystallized in toluene
出典と根拠
- ORDレコード
- ord-20f53bdf122d4c0eb79fea6119fe9f55
- 出典データセット
- uspto-grants-1993_09
- 特許番号
- US05246951
反応ノート
読み込み中…