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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071206Generated: November 1, 2026

4-Chloro-2-(propan-2-yl)-1H-indene → 4-(3,5-Dimethylphenyl)-2-isopropylindene

https://huagongshe.com/reaction/1071206

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-(propan-2-yl)-1H-indeneHCID 21918397—
ReactantHCID 178425074HCID 178425074—
CatalystHCID 178418751HCID 178418751—
SolventDiethyl EtherHCID 3283—
Product4-(3,5-Dimethylphenyl)-2-isopropylindeneHCID 22023014—

Reaction Steps

4-chloro-2-isopropylindene (10.0 g, 54 mmol) and NiCl2(PPh3)2 (1.8 g, 2.8 mmol) were dissolved in 150 mL of Et2O. 3,5-dimethylphenylmagnesium bromide (54 mmol) as a Et2O solution was added under vigorous stirring and the reaction was stirred overnight at room temperature. After overnight stirring, the reaction was slowly quenched with H2O to neutralize unreacted Grignard. The solution was subsequently treated with 100 mL of 10% HCl(aq), neutralized with saturated sodium bicarbonate aqueous solution. The organic layer was dried with magnesium sulfate and the solvent was removed by rotary evaporation. The remaining residue was loaded onto a silica gel column and eluted with hexane. Yield was 5.5 g (39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903229B2
Source datasetuspto-grants-2005_06
ORD IDord-677d24a720f4451aa85a5f97698ccda8
Source noteuspto-grants-2005_06