HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563456Generated: October 31, 2026
1-Phenylnaphthalen-2-ol → HCID 178425996, compound
https://huagongshe.com/reaction/563456
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) dissolved in 100 mL of toluene, n-butyllithium (2.5 M in hexane, 3.6 mL) was slowly injected at −78° C. After stirring the mixture at ambient temperature for 12 hours, the reaction mixture was chilled to −78° C., and solution of (pentamethylcyclopentadienyl)titanium(IV) trichloride (2.5 g, 16.3 mmol) dissolved in 60 mL of toluene was slowly added thereto, and the reaction was continued at ambient temperature for 12 hours. When the reaction was completed, the reaction mixture was filtered through celite, and the solvent was removed. Recrystallization from purified toluene and hexane at −35° C., followed by filtration and drying under reduced pressure gave (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 |
|---|
| Patent number | US08067511B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-72025fc055df4c0f8f1b111316d4f66a |
|---|
| Source note | uspto-grants-2011_11 |
|---|