Bicyclo[2.2.2]oct-5-en-2-one → Bicyclo[4.2.0]oct-3-en-7-one
Reaction equation
[CH:1]12[CH2:8][CH2:7][CH:4]([CH:5]=[CH:6]1)[CH2:3][C:2]2=[O:9]>C1CCCCC1>[CH:5]12[C:2](=[O:9])[CH2:3][CH:4]1[CH2:7][CH:8]=[CH:1][CH2:6]2Participants
3
Reagents, catalysts & solvents 1
Procedure
A 4% solution of (+)-bicyclo[2.2.2]oct-5-en-2-one was dissolved in cyclohexane and irradiated in a Pyrex apparatus under argon with a 250 w. medium pressure mercury lamp. After 50 hours, the starting product had been reacted quantitatively. The solution was concentrated by evaporation and the residue subjected to chromatography on 100 g. of silica gel with toluene/1% diethyl ether. Pure (-)-bicyclo[4.2.0]oct-3-en-8-one was obtained.
Workup
- customirradiated in a Pyrex apparatus under argon with a 250 w
- customthe starting product had been reacted quantitatively
- concentrationThe solution was concentrated by evaporation
Sources & evidence
- ORD record
- ord-1bebd9bd0a114af5b15ba0879c203486
- Source dataset
- uspto-grants-1984_07
- Patent number
- US04461687
Reaction notes
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