反応式
[C:1]1([C:7]2[CH:8]=[CH:9][CH:10]=[C:11]3[C:15]=2[NH:14][C:13](=[O:16])[CH2:12]3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-:17].[Na+]>>[OH2:16].[NH2:14][C:15]1[C:11]([CH2:12][C:13]([OH:16])=[O:17])=[CH:10][CH:9]=[CH:8][C:7]=1[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
3
実験手順
A mixture of 4.5 g. (0.0215 mole) of 7-phenylindolin-2-one and 60 ml. of 3N sodium hydroxide was heated at reflux under nitrogen for 17 hrs. The reaction mixture was cooled, filtered, and the filtrate was diluted with 60 ml. of water. The solution was cooled, made acidic with glacial acetic acid and the resulting tan solid was immediately collected by filtration, washed with cold water and dried under vacuum to yield 4.6 g. (98%) of product as a tan solid, m.p. 98°-100° C. (dec.).
後処理
- additionA mixture of 4.5 g
- temperatureat reflux under nitrogen for 17 hrs
- temperatureThe reaction mixture was cooled
- filtrationfiltered
- additionthe filtrate was diluted with 60 ml
- temperatureThe solution was cooled
- filtrationthe resulting tan solid was immediately collected by filtration
- washwashed with cold water
- customdried under vacuum
- customto yield 4.6 g
出典と根拠
- ORDレコード
- ord-810bec54eeb64820b53974d38f8faaf2
- 出典データセット
- uspto-grants-1987_06
- 特許番号
- US04670566
関連ノート
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