Hydrogen Peroxide → 2-Cyclohexylmethyl-4-morpholin-4-yl-4-oxobutyric acid

HRID 1060746ノート

反応式

HRID 1060746 の反応式
[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]1

参加物

6

実験手順

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%).

後処理

  1. stirringstirred for an additional 30 minutes
  2. customThe organic solvent was removed under reduced pressure
  3. additionthe residual mixture was diluted with water (30 mL)
  4. extractionThe dilution was extracted with methylene chloride (3×30 mL)
  5. extractionextracted with dichloromethane (3×20 mL)
  6. dry with materialThe combined extracts were dried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated to dryness

出典と根拠

ORDレコード
ord-4d1c535ebe044a4b9b77efab639365e4
出典データセット
uspto-grants-2003_02
特許番号
US06525036B2

反応ノート

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