反応式
[CH3:1][O:2][C:3]1[CH:13]=[CH:12][C:6]2[CH:7]=[CH:8][CH2:9][Te:10](=[O:11])[C:5]=2[CH:4]=1.[F:14][S:15]([O:18][CH2:19][CH3:20])(=[O:17])=[O:16]>CCOCC>[F:14][S:15]([OH:18])(=[O:17])=[O:16].[CH2:19]([O:18][C:7]1[C:6]2[CH:12]=[CH:13][C:3]([O:2][CH3:1])=[CH:4][C:5]=2[Te:10](=[O:11])[CH2:9][CH:8]=1)[CH3:20]参加物
4
反応条件
- 温度
- 60 °C
実験手順
Five g of 7-methoxybenzotelluropyrone was added to 20 ml of freshly distilled ethyl fluorosulfonate. The resulting mixture was stirred under nitrogen at 60° C. for 10 minutes. Two hundred ml of ether was added precipitating a red solid. The product was collected by filtration and recrystallized from acetonitrile to give 6.0 g (87%) of a red solid.
後処理
- customprecipitating a red solid
- filtrationThe product was collected by filtration
- customrecrystallized from acetonitrile
出典と根拠
- ORDレコード
- ord-43b52567e692450fa38bf11e977429f0
- 出典データセット
- uspto-grants-1982_12
- 特許番号
- US04365017
関連ノート
読み込み中…