Potassium Carbonate → 3,3a,4,5,6,6a-hexahydro-2H-pentalen-1-one

HRID 462792Notes

Reaction equation

HRID 462792 reaction equation
[OH:1][CH:2]1[CH2:9][CH2:8][CH:7]2[CH:3]1[CH2:4][CH2:5][CH2:6]2.C([O-])(=O)C.[K+].C(=O)([O-])[O-].[K+].[K+].[Cr](Cl)([O-])(=O)=O.[NH+]1C=CC=CC=1>ClCCl>[CH:7]12[CH2:8][CH2:9][C:2](=[O:1])[CH:3]1[CH2:4][CH2:5][CH2:6]2

Participants

6

Conditions

Temperature
20 °C

Procedure

A stirred solution of (E)-2-[(mixture of 3α and 3β)-tert-butyldimethylsilyloxyoct-1-enyl]-6-hydroxybicyclo[3,3,0]octane (430 mg prepared as described in Reference Example 25 and predominantly in the 2β-configuration) in dry dichloromethane (15 ml) was treated with potassium acetate (127 mg), potassium carbonate (110 mg) and pyridinium chlorochromate (561 mg), and the mixture was stirred for 150 minutes at 20° C. A further quantity of pyridinium chlorochromate (120 mg) was then added and the mixture was stirred for a further period of 1 hour. The mixture was then concentrated in vacuo and subjected to chromatography on a silica gel column, using a mixture of ethyl acetate and hexane (1:4 v/v) as eluant, to give (E)-2-[(mixture of 3α and 3β)-tertbutyldimethylsilyloxyoct-1-enyl]bicyclo[3,3,0]octan-6-one (330 mg), predominantly in the 2β-configuration.

Workup

  1. stirringthe mixture was stirred for a further period of 1 hour
  2. concentrationThe mixture was then concentrated in vacuo
  3. additiona mixture of ethyl acetate and hexane (1:4 v/v) as eluant

Sources & evidence

ORD record
ord-a8d5f42dbc864175ac76d2ea70bd6ad7
Source dataset
uspto-grants-1985_05
Patent number
US04517202

Reaction notes

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