Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thymol | HCID 6989 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178421920 | HCID 178421920 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178421918 | HCID 178421918 | — |
Reaction Steps
3.2 g (21 mmol) of 2-isopropyl-5-methylphenol in 20 ml of toluene/2 ml of THF were admixed at room temperature with 7.8 ml (21 mmol) of a 20% strength solution of butyllithium in toluene. The mixture was stirred for another 1 hour at 60° C. At room temperature, 5.0 g (10.5 mmol) of dimethylsilanediylbis(2-methylindenyl)zirconium dichloride were added as a solid. The suspension was stirred at 100° C. for 2 hours and subsequently filtered hot through Celite. The filter cake was extracted twice with 25 ml each time of toluene (100° C.). After evaporation of the solvent, the yellow solid which had precipitated was filtered off and dried under reduced pressure. This gave 1.36 g (22%) of dimethylsilanediylbis(2-methylindenyl)zirconium monochloride mono(2-isopropyl-5-methylphenoxide) (4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06900343B1 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-60060db7ab9c47f8898527bfb5985050 |
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| Source note | uspto-grants-2005_05 |
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