2,6-Lutidine → (7a-Methyl-1,5-dioxo-octahydro-inden-4-yloxy)-acetaldehyde
Reaction equation
[CH2:1]([O:4][CH:5]1[C:13](=[O:14])[CH2:12][CH2:11][C:10]2([CH3:15])[CH:6]1[CH2:7][CH2:8][C:9]2=[O:16])[CH:2]=C.N1C(C)=CC=CC=1C.I([O-])(=O)(=O)=[O:26].[Na+]>O1CCOCC1.O.[Os](=O)(=O)(=O)=O>[CH3:15][C:10]12[C:9](=[O:16])[CH2:8][CH2:7][CH:6]1[CH:5]([O:4][CH2:1][CH:2]=[O:26])[C:13](=[O:14])[CH2:12][CH2:11]2Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 3
Procedure
A commercial 4% w/w solution of osmium tetraoxide (10 mL, 0.82 mmol, 0.005 eq) was added to a stirred mixture of 4-allyloxy-7a-methyl-hexahydro-indene-1,5-dione (36.4 g, 164 mmol), 2,6-lutidine (57.2 mL, 246 mmol, 1.5 eq) and sodium periodate (210.6 g, 492 mmol, 3 eq) in dioxane (900 mL) and water (300 mL) at 0° C. The reaction mixture was then allowed to warm slowly to room temperature, and stirred for 24 h. The reaction mixture was cooled to 0° C., and then filtered through a fritted funnel. DCM (1 L) was used to wash to salt cake, and the filtrate was used to extract the separated aqueous solution (4×250 mL). The combined organic layer was dried with magnesium sulfate. The resulting mixture was filtered, condensed and the resulting residue purified by flash chromatography using 20-90% ethyl acetate in hexane yield the title compound as a light yellow foam.
Workup
- temperatureThe reaction mixture was cooled to 0° C.
- filtrationfiltered through a fritted funnel
- washto wash to salt cake
- extractionto extract the separated aqueous solution (4×250 mL)
- dry with materialThe combined organic layer was dried with magnesium sulfate
- filtrationThe resulting mixture was filtered
- customcondensed
- customthe resulting residue purified by flash chromatography
Sources & evidence
- ORD record
- ord-132bd8ebdaa34940ad59cac16ebed7f0
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07763648B2
Reaction notes
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