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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838513Generated: October 28, 2026

Carbazole → HCID 178478525, compound

https://huagongshe.com/reaction/1838513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbazoleHCID 6854—
ReactantZirconium chloride (ZrCl4), (T-4)-HCID 9856075—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
ProductHCID 178478525HCID 178478525—

Reaction Steps

Complex Preparation (Steps 1 and 2). Carbazole (5.0 g, 30 mmol) is stirred in a flask under an atmosphere of nitrogen in a dry box for 15 min. Toluene (120 mL) is added, and the mixture is stirred for 30 min. n-Butyllithium (12 mL of 2.5 M solution in hexane, 30 mmol) is added by syringe over 5 min. to the stirred carbazole solution. The mixture is stirred at room temperature for 2 h. The mixture turns light pink, and the slurry becomes thick, requiring vigorous stirring. Zirconium tetrachloride (3.50 g, 15 mmol) and more toluene (25 mL) are added to the flask, and the mixture turns brown. Stirring is continued at room temperature for another 18 h, after which the mixture is black-brown-green. Solvents are removed under a flow of nitrogen, and the residue is vacuum dried for 3 h. A yellow solid (9.25 g) that contains 81 wt. % of the desired bis(carbazolyl) complex (15.1 wt. % Zr) is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673882B2
Source datasetuspto-grants-2004_01
ORD IDord-8be2faf9418c4a97b3fcbed062578821
Source noteuspto-grants-2004_01