Acetic Anhydride → 1-Acetyl-5-fluoro-1,3-dihydro-indol-2-one
反応式
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:11])[CH2:5]2.[C:12](OC(=O)C)(=[O:14])[CH3:13]>>[C:12]([N:7]1[C:8]2[C:4](=[CH:3][C:2]([F:1])=[CH:10][CH:9]=2)[CH2:5][C:6]1=[O:11])(=[O:14])[CH3:13]参加物
3
実験手順
At 170° C. 3.0 g (20 mmol) 5-fluoroindolinone were stirred for 3 h in 10 mL (98 mmol) acetic anhydride. After cooling to RT the mixture was poured onto 200 mL ice water, the precipitated substance was suction filtered and washed with 100 mL water. The solid was recrystallised from 100 mL water and 50 mL ethanol at boiling temperature. The precipitated product was suction filtered, washed with 30 mL water and dried in the CAD.
後処理
- customAt 170° C
- filtrationfiltered
- washwashed with 100 mL water
- customThe solid was recrystallised from 100 mL water and 50 mL ethanol
- filtrationfiltered
- washwashed with 30 mL water
- customdried in the CAD
出典と根拠
- ORDレコード
- ord-5e3192e3dfd249f69143016f8f40d71d
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08829006B2
反応ノート
読み込み中…