Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | Sodium Sulfate | HCID 24436 | — |
| Edukt | 4,7-Dimethyl-1-indanone | HCID 220094 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 4,7-Dimethyl-1-indanol | HCID 15877605 | — |
| Edukt | Aluminium lithium hydride | HCID 21226445 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4,7-dimethyl-1H-indene | HCID 81458 | 91,9% |
Reaktionsschritte
2.9 g (0.0181 moles) of 4,7-dimethyl-1-indanone (formula XVII) obtained as described above, are slowly added to a suspension of 0.350 g (0.0692 moles) of LiAlH4 in 30 ml of ethyl ether, maintained at −30° C. in an inert atmosphere. The reaction is complete after 30 minutes. Ice and HCl 2N are cautiously added until acidification, the mixture is then extracted with ethyl ether, and the organic phase is subsequently separated and washed until neutrality. It is anhydrified on sodium sulfate and evaporated, obtaining a residue essentially consisting of 4,7-dimethyl-1-indanol. The residue is dissolved in 10 ml of THF, a pinch of p-toluenesulfonic acid is added and the mixture is brought to reflux temperature for 1 hour. Solid NaHCO3 and Na2SO4 are then added. The mixture is filtered and the solvent evaporated obtaining 2.4 g of 4,7-dimethylindene (XVIII) (91% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06211110B1 |
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| Quelldatensatz | uspto-grants-2001_04 |
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| ORD ID | ord-0aa9780815a7402c8577ecf3c21be3fa |
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| Quellennotiz | uspto-grants-2001_04 |
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