反応式
F[C:2]1[C:19](F)=[CH:18][C:17]2[C:16](=[O:21])[C:15]3[C:6](=[CH:7][C:8]4[C:13]([CH:14]=3)=[CH:12][CH:11]=[CH:10][CH:9]=4)[C:5](=[O:22])[C:4]=2[CH:3]=1.[C:23]([O-:26])([O-])=O.[K+].[K+].[CH3:29][OH:30].Cl>CS(C)=O>[CH3:29][O:30][C:2]1[C:19]([O:26][CH3:23])=[CH:18][C:17]2[C:16](=[O:21])[C:15]3[C:6](=[CH:7][C:8]4[C:13]([CH:14]=3)=[CH:12][CH:11]=[CH:10][CH:9]=4)[C:5](=[O:22])[C:4]=2[CH:3]=1参加物
6
実験手順
1 g (3.4 mmol) of 2,3-difluoro-naphthacene-5,12-dione, 0.94 g (6.8 mmol) of K2CO3, 2.18 g of methanol and 20 ml of DMSO are stirred at 110° C. for 22 hours. The mixture is poured onto dilute hydrochloric acid. The product is filtered off, washed four times with water, dried and recrystallized from CH2Cl2 /pentane; yield 0.72 g (67%); melting point >250° C.
後処理
- filtrationThe product is filtered off
- washwashed four times with water
- customdried
- customrecrystallized from CH2Cl2 /pentane
出典と根拠
- ORDレコード
- ord-e5097bd68377463983c1e1c315f75eae
- 出典データセット
- uspto-grants-1995_02
- 特許番号
- US05391749
関連ノート
読み込み中…