Reaktion #409101

Reaktionsgleichung

n-BuLi

4,7-dimethyl indene

4,7-dimethylindene

water

→

1-(4,7-dimethyl-1-indenyl)-2-(4,7-dimethyl-1-indenyl)methyl benzene

Lösungsmittel

THF hexane

—

mixture

hexane

THF hexane

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONAt the end of the addition
2. 2
   workup.WAITthe mixture is left
3. 3
   workup.ADDITIONare added dropwise
4. 4
   workup.WAITThe mixture is left
5. 5
   Sonstigeto rise to room temperature
6. 6
   workup.WAITis left
7. 7
   workup.WAITto rest for 6 hours
8. 8
   Extraktionis extracted with ethyl ether
9. 9
   WaschenThe organic phase is washed until neutrality
10. 10
    SonstigeThe residue obtained by evaporation of the solvent
11. 11
    Sonstigeis purified by silica gel chromatography
12. 12
    SonstigeAfter evaporation of the eluant 2.0 g of the bis-indenyl ligand
13. 13
    Sonstigeare obtained (72% yield)

Vorschrift

4.12 ml (10.3 mmoles) of n-BuLi 2.5 M in hexane are added to a solution of 1.48 g of 4,7-dimethyl indene (XVIII) (10.3 mmoles; obtained as described above) in 55 ml of a mixture of THF-hexane 2/1. At the end of the addition, the mixture is left under stirring for 1 hour. It is then cooled to −70° C. and a solution of 2.3 g of the brominated compound having formula (XX) (7.37 mmoles) in THF/hexane are added dropwise. The mixture is left to rise to room temperature and is left to rest for 6 hours. It is then poured into water and is extracted with ethyl ether. The organic phase is washed until neutrality and dehydrated on sodium sulfate. The residue obtained by evaporation of the solvent is purified by silica gel chromatography eluating with petroleum ether. After evaporation of the eluant 2.0 g of the bis-indenyl ligand having formula (XXI) and indicated below, are obtained (72% yield).

Quelle