Sodium Carbonate → HCID 70396540, compound

HRID 1722386Notes

Reaction equation

HRID 1722386 reaction equation
[OH:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH:7]1[CH2:14][CH2:13][CH:12]2[CH:8]1[CH2:9][C:10](=[O:15])[CH2:11]2.C(=O)([O-])[O-:17].[Na+].[Na+].[Mn]([O-])(=O)(=O)=O.[K+]>>[C:2]([CH2:3][CH2:4][CH2:5][CH:6]=[C:7]1[CH2:14][CH2:13][CH:12]2[CH:8]1[CH2:9][C:10](=[O:15])[CH2:11]2)([OH:17])=[O:1]

Participants

4

Procedure

2-(5-Hydroxypent-1-yl)bicyclo[3.3.0]octan-7-one {hexahydro-4-(5-hydroxyheptyl)-2(1H)-pentalenone} (0.5 g, 2.4 mmoles) is mixed with a 10% solution of sodium carbonate (0.51 ml). The reaction is cooled in an ice bath and solution of potassium permanganate (0.48 g dissolved in 12 ml water) is slowly added over 10 minutes. The ice bath is then removed and the reaction mixture stirred at room temperature for 12 hour, after which time the precipitated manganese dioxide is filtered off and the filtrate partitioned between ether. The solution is acidified with dilute sulfuric acid and the organic layer separated. The aqueous phase is extracted with ether (2×20 ml), and the ether extracts combined and dried over anhydrous sodium sulfate. The solvent is removed under vacuum leaving a clear colorless oil. The crude product is chromatographed on silica gel and subsequently kugelrohred under reduced pressure leaving a clear, colorless oil (0.050 g, 0.22 mmoles).

Workup

  1. temperatureThe reaction is cooled in an ice bath
  2. customThe ice bath is then removed
  3. filtrationafter which time the precipitated manganese dioxide is filtered off
  4. customthe filtrate partitioned between ether
  5. customthe organic layer separated
  6. extractionThe aqueous phase is extracted with ether (2×20 ml)
  7. dry with materialdried over anhydrous sodium sulfate
  8. customThe solvent is removed under vacuum
  9. customleaving a clear colorless oil
  10. customThe crude product is chromatographed on silica gel

Sources & evidence

ORD record
ord-0da9d4e07a9e4c059c969b4d7d1d2972
Source dataset
uspto-grants-1989_08
Patent number
US04855322

Reaction notes

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