反応式
[SH:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([OH:11])=[O:10])=[CH:4][CH:3]=1.[OH-].[K+].Br[C:15]1[S:19][C:18]([S:20]([NH2:23])(=[O:22])=[O:21])=[CH:17][CH:16]=1>CN(C)C=O.O>[C:9]([CH2:8][C:5]1[CH:4]=[CH:3][C:2]([S:1][C:15]2[S:19][C:18]([S:20]([NH2:23])(=[O:22])=[O:21])=[CH:17][CH:16]=2)=[CH:7][CH:6]=1)([OH:11])=[O:10]参加物
6
反応条件
- 温度
- 120 °C
実験手順
4-Mercaptophenylacetic acid (2.3 g) was dissolved in dimethylformamide under a nitrogen atmosphere and 1.8 g of potassium hydroxide dissolved in a minimum amount of water was added. 5-bromothiophene-2-sulfonamide (3.3 g) dissolved in dimethylformamide was added and the mixture heated at 120° C. for 2 hours. After cooling to room temperature water was added to the reaction mixture, the pH was adjusted to 8.6 and the mixture was extracted with ethyl acetate. The aqueous phase was separated and acidified, causing a solid to precipitate. The solid was collected by filtration and dried under vacuum to a weight of 3.25 g.
後処理
- additionwas added
- additionwas added
- additionwas added to the reaction mixture
- extractionthe mixture was extracted with ethyl acetate
- customThe aqueous phase was separated
- customto precipitate
- filtrationThe solid was collected by filtration
- customdried under vacuum to a weight of 3.25 g
出典と根拠
- ORDレコード
- ord-e9ec0aeb8d5c4266906869950d3ea639
- 出典データセット
- uspto-grants-1989_07
- 特許番号
- US04847289
関連ノート
読み込み中…