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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907501Generated: October 29, 2026

Toluene → HCID 178455874, compound

https://huagongshe.com/reaction/907501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant1-(Prop-2-en-1-yl)-1H-indeneHCID 247600—
ReactantHCID 178486194HCID 178486194—
ProductHCID 178455874HCID 178455874—

Reaction Steps

To Tetrakis(dimethylamino)zirconium (0.52 g, 1.94 mmol) dissolved in toluene (6 mL) was added allylindene (0.31 g, 1.99 mmol) at room temperature. The mixture was stirred at room temperature overnight. To the mixture was added Me3SiCl (1 mL, 7.9 mmol) at room temperature. The mixture was stirred at room temperature overnight. Removal of the solvent gave a yellow solid (crude allylindenylzirconium trichloride). The yellow solid (crude allylindenylzirconium trichloride) was dissolved in THF (10 mL). N-BuCpLi (0.276 g, 2.15 mmol) dissolved in THF (6 mL) was added to above THF solution (allylindenylzirconium trichloride/THF solution) at 0° C. The mixture was stirred at 0° C. for 30 minutes, then warned to room temperature and stirred for another 2.5 hours. The solvent was removed. The residue was extracted with toluene (30 mL). The supernatant was separated from the solid. Removal of the solvent gave a yellow solid. The yellow solid was washed with pentane (30 mL) and then dried under vacuum. The desired compound was obtained as a pale yellow solid (0.54 g, 64% overall yield). The product was identified by 1H-NMR (FIG. 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08013177B2
Source datasetuspto-grants-2011_09
ORD IDord-20670803e3fc462088f4c2682ee21e02
Source noteuspto-grants-2011_09