HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178478629, compound → HCID 178528074, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178478629 | HCID 178478629 | — |
| Reactant | HCID 178506658 | HCID 178506658 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178528074 | HCID 178528074 | — |
Reaction Steps
A sample of the indeno[1,2-b]indolyl lithium salt produced above (10 g, 42 mmol) is dissolved in toluene (95 mL) to produce an orange slurry. Diethyl ether (35 mL) is added slowly to give an orange solution. This solution is added over 15 min. at room temperature with stirring to a slurry of cyclopentadienylzirconium trichloride (11 g, 42 mmol) in toluene (190 mL) and diethyl ether (190 mL). The mixture turns deep red and is kept at room temperature overnight. The slurry is filtered to recover a red solid, which is washed with toluene (200 mL) and dried under vacuum. Yield of complex 10: 16.5 g. The 1H NMR spectrum is consistent with the proposed structure:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06838410B2 |
| Source dataset | uspto-grants-2005_01 |
| ORD ID | ord-104824d793ea47af853a212c5ecfdd3a |
| Source note | uspto-grants-2005_01 |