Hydrogen Peroxide → HCID 22915511、化合物
反応式
[C:1]([O:5][C:6]([CH2:8][CH:9]([CH2:25][CH2:26][O:27][C:28]1[CH:33]=[CH:32][C:31]([C:34]2[CH:39]=[CH:38][C:37]([C:40]#[N:41])=[CH:36][CH:35]=2)=[CH:30][CH:29]=1)C(N1[C@@H](CC2C=CC=CC=2)COC1=O)=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].[OH:42]O.[Li+].[OH-].C1[CH2:50][O:49]CC1>>[C:1]([O:5][C:6]([CH2:8][CH:9]([CH2:25][CH2:26][O:27][C:28]1[CH:29]=[CH:30][C:31]([C:34]2[CH:39]=[CH:38][C:37]([C:40]#[N:41])=[CH:36][CH:35]=2)=[CH:32][CH:33]=1)[C:50]([OH:49])=[O:42])=[O:7])([CH3:3])([CH3:4])[CH3:2]参加物
反応条件
- 温度
- 0 °C
実験手順
To a 0° C. solution in THF (200 mL) of N-[2-tert-butyloxycarbonylmethyl-4-(4-(4-cyanophenyl)phenoxy)butanoyl]-(S)-(-)-4-benzyl-2-oxazolidinone (7.05 g, 12.7 mmol) was added 30% aqueous H2O2 (3.0 mL, 50.8 mmol) and 1M aqueous LiOH (20.3 mL, 20.3 mmol) and the reaction mixture was stirred for one hour. The reaction mixture was quenched with saturated aqueous NaHSO3 and diluted with dichloromethane. The aqueous phase was made basic with aqueous 2N NaOH and extracted twice with dichloromethane. The organic extracts were discarded and the aqueous phase was cooled to 0° C. and acidified with aqueous 2N HCl. The aqueous phase was extracted with dichloromethane and THF/dichloromethane. The combined organic extracts were dried over MgSO4, filtered, and concentrated in vacuo. Chromatography on silica gel (dichloromethane/10% THF/1% methanol) gave 2-tert-butyloxycarbonylmethyl-4-[4-(4-cyanophenyl)phenoxy]butanoic acid (2.6 g, 52%).
後処理
- customThe reaction mixture was quenched with saturated aqueous NaHSO3
- additiondiluted with dichloromethane
- extractionextracted twice with dichloromethane
- extractionThe aqueous phase was extracted with dichloromethane and THF/dichloromethane
- dry with materialThe combined organic extracts were dried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-4ae1e2cafa234b70a2d6f48eb77bfff1
- 出典データセット
- uspto-grants-1997_09
- 特許番号
- US05665777
反応ノート
読み込み中…