Sulfuric Acid → 4-(Methylsulfonyl)phenol
反応式
C1[C:6]([C@H:7]([CH2:12][NH2:13])[CH2:8][C:9]([OH:11])=[O:10])=[CH:5][CH:4]=C(Cl)C=1.[C:15](=[O:18])([O-:17])[O-].[K+].[K+].[CH3:21][CH:22]([CH3:44])[C:23]([O:25][CH:26](OC([O:33][C:34]1[CH:39]=[CH:38][C:37]([S:40]([CH3:43])(=[O:42])=[O:41])=[CH:36][CH:35]=1)=O)[CH:27](C)C)=[O:24].S(=O)(=O)(O)O.[C:50](#N)C>COC(C)(C)C.O>[CH3:50][CH:5]([CH3:4])[CH2:6][C@H:7]([CH2:12][NH:13][C:15]([O:17][CH2:27][CH2:26][O:25][C:23](=[O:24])[CH:22]([CH3:44])[CH3:21])=[O:18])[CH2:8][C:9]([OH:11])=[O:10].[CH3:43][S:40]([C:37]1[CH:38]=[CH:39][C:34]([OH:33])=[CH:35][CH:36]=1)(=[O:41])=[O:42]参加物
反応物 5
生成物 2
試薬・触媒・溶媒 2
実験手順
R-Baclofen (2.13 g) and water (50 mL) were charged to a vessel at room temperature. Potassium carbonate (1.6 g) was added in one portion and the mixture was stirred at room temperature for 5 minutes. A solution of 2-methyl-1-[4-(methylsulfonyl)phenoxycarbonyloxy]propyl 2-methylpropanoate D6 (3.5 g) in acetonitrile (50 mL) was added. After 6 hours, tert-butyl methyl ether (50 mL) was added and the reaction mixture was cooled to 5-10° C. A 5% aqueous sulfuric acid was added to adjust the pH to approximately 3. The mixture was then warmed to room temperature and stirred for 10 minutes. The organic layer was washed with water (3×20 mL) and evaporated to provide the crude title compound as an orange oil with 4-(methylsulfonyl)phenol impurity.
後処理
- waitAfter 6 hours
- temperaturethe reaction mixture was cooled to 5-10° C
- temperatureThe mixture was then warmed to room temperature
- stirringstirred for 10 minutes
- washThe organic layer was washed with water (3×20 mL)
- customevaporated
出典と根拠
- ORDレコード
- ord-037d556ae9d74d86ab682802c1ce4935
- 出典データセット
- uspto-grants-2012_10
- 特許番号
- US08299291B2
反応ノート
読み込み中…