HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387492Generated: October 30, 2026
1-Phenylnaphthalen-2-ol → HCID 178425996, compound
https://huagongshe.com/reaction/387492
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Phenylnaphthalen-2-ol | HCID 11218282 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178425990 | HCID 178425990 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178425996 | HCID 178425996 | 58.2% |
Reaction Steps
To solution of 1-phenylnaphthalen-2-ol (2.0 g, 9.1 mmol) in toluene (100 mL), slowly injected was n-butyllithium (2.5 M in hexane, 3.6 mL) at −78° C., and the mixture was stirred at ambient temperature for 12 hours. After chilling the reaction mixture to −78° C., slowly added was solution of (pentamethylcyclopentadienyl)titanium(IV) trichloride (2.5 g, 16.3 mmol) in toluene (60 mL), and the reaction was carried out at ambient temperature for 12 hours. When the reaction was completed, the reaction mixture was filtered through a celite filter, and solvent was removed therefrom. Recrystallization was carried out from purified toluene and hexane at −35° C. The solid was filtered and dried under reduced pressure to obtain (dichloro)(pentamethylcyclopentadienyl)(1-phenylnaphthalen-2-yloxy)titanium(IV) (2.5 g, yield: 58.2%) as red solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372996B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-91c056dc4c8a41ac9c237cd1f9778e6a |
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| Source note | uspto-grants-2013_02 |
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