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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411781Generated: October 30, 2026

HCID 178478629, compound → HCID 178528074, compound

https://huagongshe.com/reaction/411781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178478629HCID 178478629—
ReactantHCID 178506658HCID 178506658—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 178528074HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559251B1
Source datasetuspto-grants-2003_05
ORD IDord-7c5930c9bdd44d4aa67a504df3453fe2
Source noteuspto-grants-2003_05