Hydrogen Peroxide → 2-Cyclohexylmethyl-4-morpholin-4-yl-4-oxobutyric acid
반응식
[CH:1]1([CH2:7][CH:8]([CH2:20][C:21]([N:23]2[CH2:28][CH2:27][O:26][CH2:25][CH2:24]2)=[O:22])[C:9](N2C(C(C)C)COC2=O)=[O:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.O.[OH-].[Li+].OO.N([O-])=[O:35].[Na+]>C1COCC1>[CH:1]1([CH2:7][CH:8]([CH2:20][C:21]([N:23]2[CH2:28][CH2:27][O:26][CH2:25][CH2:24]2)=[O:22])[C:9]([OH:10])=[O:35])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
A solution of 2-cyclohexylmethyl-1-(4-isopropyl-2-oxooxazolidin-3-yl)-4-morpholin-4-yl-butane-1,4-dione (1.63 g, 4.13 mmol) in THF (20 mL) was treated with lithium hydroxide monohydrate (0.226 g, 5.37 mmol) and hydrogen peroxide (2 mL of a 30% solution) and the mixture was stirred overnight at ambient temperature. The mixture was treated with sodium nitrite (1.3 g) and stirred for an additional 30 minutes. The organic solvent was removed under reduced pressure and the residual mixture was diluted with water (30 mL). The dilution was extracted with methylene chloride (3×30 mL) and the aqueous layer was acidified to pH 2 with 1M hydrochloric acid and extracted with dichloromethane (3×20 mL). The combined extracts were dried (MgSO4), filtered and concentrated to dryness to provide 2-cyclohexylmethyl-4-morpholin-4-yl-4-oxobutyric acid (0.56 g, 48%).
후처리
- stirringstirred for an additional 30 minutes
- customThe organic solvent was removed under reduced pressure
- additionthe residual mixture was diluted with water (30 mL)
- extractionThe dilution was extracted with methylene chloride (3×30 mL)
- extractionextracted with dichloromethane (3×20 mL)
- dry with materialThe combined extracts were dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated to dryness
출처 및 근거
- ORD 기록
- ord-4d1c535ebe044a4b9b77efab639365e4
- 출처 데이터셋
- uspto-grants-2003_02
- 특허 번호
- US06525036B2
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