Sodium Sulfite → HCID 69081664, compound

HRID 1761171Notes

Reaction equation

HRID 1761171 reaction equation
C([O:4][C:5]1[CH2:9][C@H:8]([C@@:10]2([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[C:14](=[O:15])[O:13][C@H:12]([C:16]([CH3:19])([CH3:18])[CH3:17])[O:11]2)[CH2:7][CH:6]=1)(=O)C.C[N+]1([O-])CC[O:30]CC1.S([O-])([O-])=O.[Na+].[Na+]>C(#N)C.O.C(OCC)(=O)C.[Os](=O)(=O)(=O)=O>[C:16]([C@H:12]1[O:13][C:14](=[O:15])[C@@:10]([C@H:8]2[CH2:7][C:6](=[O:30])[C@H:5]([OH:4])[CH2:9]2)([C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)[O:11]1)([CH3:17])([CH3:18])[CH3:19]

Participants

8

Procedure

To a solution of 169 mg of (4R)-4-((2R,4R)-2-(t-butyl)-5-oxo-4-phenyl-1,3-dioxolan-4-yl)-1-cyclopentenyl acetate in 7.5 ml of acetonitrile and water (2:1), 80 mg of N-methyl morpholine-oxide and 0.2 ml of 2% aqueous osmium tetraoxide solution were successively added at 0° C. by the order stated, followed by 3 hours' stirring at the same temperature. Sodium sulfite was added to the reaction liquid and stirred for further 30 minutes. The reaction liquid was then diluted with ethyl acetate, washed successively with water and saturated brine, and dried over anhydrous sodium sulfate. Distilling the solvent off under reduced pressure, the residue obtained was purified on silica gel column chromatography (eluent: hexane−hexane/ethyl acetate=2/1) to provide 32 mg of the title compound as a colorless solid.

Workup

  1. stirringstirred for further 30 minutes
  2. customThe reaction liquid
  3. washwashed successively with water and saturated brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. distillationDistilling the solvent off under reduced pressure
  6. customthe residue obtained
  7. customwas purified on silica gel column chromatography (eluent: hexane−hexane/ethyl acetate=2/1)

Sources & evidence

ORD record
ord-342b45e79b424a53b64f9a5e0224f66a
Source dataset
uspto-grants-2005_01
Patent number
US06846835B2

Reaction notes

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