HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172149Generated: November 1, 2026
2,6-Di-tert-butylphenol → HCID 178425998, compound
https://huagongshe.com/reaction/1172149
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Di-tert-butylphenol | HCID 31405 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178425993 | HCID 178425993 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178425998 | HCID 178425998 | 69.4% |
Reaction Steps
After 600 mg of 2,6-di-tert-butylphenol (2.91 mmol) (Aldrich, 99%) were dissolved in 30 mL of diethylether, 1.28 mL of butyl lithium (2.5 M hexane solution) were slowly dropped thereonto at −31° C. After 1 hour, agitation was conducted at normal temperature for 6 hours. The resulting mixture was dissolved in diethylether, and a solution in which (trichloro)(pentamethylcyclopentadienyl)titanium(IV) (752 mg, 2.60 mmol) was dissolved in 10 mL of diethylether was slowly dropped thereonto at −30° C. After 1 hour, agitation was conducted at normal temperature for 6 hours. The solvent was removed from the resulting product, and the solvent-free product was dissolved in 10 mL of toluene and then recrystallized to produce 829 mg of red solid component.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07833926B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-2b334a5084bd4a3988c69641c1d4e7a1 |
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| Source note | uspto-grants-2010_11 |
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