HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827255Generated: October 30, 2026
2,4-Di-tert-butylphenol → HCID 178441055, compound
https://huagongshe.com/reaction/1827255
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Di-tert-butylphenol | HCID 7311 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178421920 | HCID 178421920 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178441055 | HCID 178441055 | — |
Reaction Steps
1.03 g (5 mmol) of 2,4-di-tert-butylphenol in 10 ml of toluene/1 ml of THF were admixed at room temperature with 1.85 ml (5 mmol) of a 20% strength solution of butyllithium in toluene. The mixture was stirred for another 1 hour at 60° C. At room temperature, 1.19 g (2.5 mmol) of dimethylsilanediylbis-(2-methylindenyl)zirconium dichloride were added as a solid. The suspension was stirred for 2 hours at 60° C. and subsequently filtered hot through Celite. The filter cake was extracted 3 times with 10 ml each time of toluene (60° C.). After evaporation of part of the solvent, the yellow solid which precipitated was filtered off and dried under reduced pressure. This gave 0.87 g (53%) of dimethylsilanediylbis(2-methylindenyl)zirconium monochloride mono(2,4-di-tert-butylphenoxide) (2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07053160B1 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-4f5866be24064ca18364ea1eabce20ca |
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| Source note | uspto-grants-2006_05 |
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