Hydrochloric Acid → 7-(2-Fluorobenzoyl)-indolin-2-one
反応式
[F:1][C:2]1[CH:21]=[CH:20][CH:19]=[CH:18][C:3]=1[C:4]([C:6]1[CH:7]=[CH:8][CH:9]=[C:10]2[C:14]=1[NH:13][C:12](=[O:15])[CH:11]2SC)=[O:5].[Sn].Cl>C(O)C>[F:1][C:2]1[CH:21]=[CH:20][CH:19]=[CH:18][C:3]=1[C:4]([C:6]1[CH:7]=[CH:8][CH:9]=[C:10]2[C:14]=1[NH:13][C:12](=[O:15])[CH2:11]2)=[O:5]参加物
5
実験手順
A mixture of 60 g (0.2 mole) of 7-(2-fluorobenzoyl)-3-methylthioindolin-2-one and 60 g (0.5 mole) of tin powder in one liter of 95% ethanol was heated to reflux and 150 ml of concentrated hydrochloric acid was added. Heating was continued for 18 hrs, then the mixture was cooled and the precipitate was collected by decanting the slurry from the remaining tin and filtering the slurry. The filter cake was recrystallized twice from absolute ethanol to give 31 g (60%) white needles, m.p. 209°-210° C.
後処理
- temperaturewas heated
- temperatureto reflux
- temperatureHeating
- temperaturethe mixture was cooled
- customthe precipitate was collected
- customby decanting the slurry from the remaining tin
- filtrationfiltering the slurry
- customThe filter cake was recrystallized twice from absolute ethanol
出典と根拠
- ORDレコード
- ord-9c96ec57725541ba8227d135cad2204b
- 出典データセット
- uspto-grants-1985_03
- 特許番号
- US04503073
反応ノート
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