tert-Butanol → HCID 86629986, compound

HRID 1013800Notes

Reaction equation

HRID 1013800 reaction equation
[CH2:1]([C@@H:8]1[CH2:12][O:11][C:10](=[O:13])[N:9]1[C:14](=[O:33])[C@H:15]([CH2:19][C:20]1[C:25]([Cl:26])=[CH:24][C:23]([C:27]([F:30])([F:29])[F:28])=[C:22]([F:31])[C:21]=1[F:32])[CH2:16][CH:17]=C)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CC([OH:38])(C)C.I([O-])(=O)(=O)=O.[Na+]>C1COCC1.O.O=[Os](=O)(=O)=O>[CH2:1]([C@@H:8]1[CH2:12][O:11][C:10](=[O:13])[N:9]1[C:14](=[O:33])[C@H:15]([CH2:19][C:20]1[C:25]([Cl:26])=[CH:24][C:23]([C:27]([F:30])([F:28])[F:29])=[C:22]([F:31])[C:21]=1[F:32])[CH2:16][CH:17]=[O:38])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

7

Procedure

Treat a solution of (R)-4-Benzyl-3-[(S)-2-(6-chloro-2,3-difluoro-4-trifluoromethyl-benzyl)-pent-4-enoyl]-oxazolidin-2-one (Preparation 45) (0.72 g, 1.5 mmol) in THF (9 mL) and water (3 mL) with 2.5% OsO4 in tBuOH (1.5 g, 0.15 mmol). Then, add sodium periodate (0.96 g, 4.5 mmol) to the solution and stir the reaction for 4 hr at room temperature. Quench the reaction with water and extract with EtOAc. Wash the organic with 1N sodium thiosulfate and brine. Separate the organic, dry over MgSO4, filter, and remove the solvent. Purify the crude by silica gel column chromatography using Hexanes:EtOAc to elute the pure product. Remove the solvent to afford 0.60 g (82%) of desired product. MS (m/e): 490 (M+1).

Workup

  1. customthe reaction for 4 hr at room temperature
  2. customQuench
  3. customthe reaction with water
  4. extractionextract with EtOAc
  5. washWash the organic with 1N sodium thiosulfate and brine
  6. customSeparate the organic,
  7. dry with materialdry over MgSO4
  8. filtrationfilter
  9. customremove the solvent
  10. customPurify the crude by silica gel column chromatography
  11. washEtOAc to elute the pure product
  12. customRemove the solvent

Sources & evidence

ORD record
ord-d3d73d6c01dc41968933f73500413541
Source dataset
uspto-grants-2011_07
Patent number
US07981918B2

Reaction notes

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