Acetic Acid → HCID 13607950、化合物
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][CH:9]2[CH2:14][CH2:13][CH2:12][N:11]([S:15]([C:18]3[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][CH:19]=3)(=[O:17])=[O:16])[CH2:10]2)=[CH:4][CH:3]=1.OO.[OH-:27].[Na+].C(O)(=[O:31])C>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:8]([CH:9]2[CH2:14][CH2:13][CH2:12][N:11]([S:15]([C:18]3[CH:19]=[CH:20][C:21]([CH3:24])=[CH:22][CH:23]=3)(=[O:17])=[O:16])[CH2:10]2)(=[O:31])=[O:27])=[CH:6][CH:7]=1参加物
反応条件
- 温度
- 90 °C
実験手順
A mixture of 37.96 g (0.10 mole) of 3-[(4-chlorophenyl)thio]-1-[(4-methylphenyl)sulfonyl]piperidine, 300 ml of glacial acetic acid, and 61.8 g of 30% hydrogen peroxide (0.6 mole) was stirred overnight at 90° C. The reaction mixture was cooled to room temperature and diluted with ice water. The diluted mixture was made alkaline with 50% aqueous sodium hydroxide and extracted with methylene chloride. The aqueous phase was discarded. The methylene chloride phase was washed with sodium sulfite to remove traces of peroxide. The methylene chloride solution was dried over magnesium sulfate, filtered and the solvent removed in vacuo to give a yellowish white solid. Recrystallization of an aliquot of the solid from methylene chloridehexanes gave the product, m.p. 186°-187° C. in 57.2% overall yield.
後処理
- temperatureThe reaction mixture was cooled to room temperature
- extractionextracted with methylene chloride
- washThe methylene chloride phase was washed with sodium sulfite
- customto remove traces of peroxide
- dry with materialThe methylene chloride solution was dried over magnesium sulfate
- filtrationfiltered
- customthe solvent removed in vacuo
- customto give a yellowish white solid
- customRecrystallization of an aliquot of the solid from methylene chloridehexanes
- customgave the product, m.p. 186°-187° C. in 57.2% overall yield
出典と根拠
- ORDレコード
- ord-dc8b66d784434dd68b33c367b9f6d1a8
- 出典データセット
- uspto-grants-1986_06
- 特許番号
- US04593102
反応ノート
読み込み中…