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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843521Generated: October 28, 2026

4-Chloro-2-methyl-1H-indene → 4-(3',5'-Di-t-butylphenyl)-2-methylindene

https://huagongshe.com/reaction/843521

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-methyl-1H-indeneHCID 12010742—
ReactantHCID 178441125HCID 178441125—
CatalystHCID 178418751HCID 178418751—
SolventDiethyl EtherHCID 3283—
Product4-(3',5'-Di-t-butylphenyl)-2-methylindeneHCID 12010743—

Reaction Steps

4-Chloro-2-methylindene (6.1 g, 37 mmol) and NiCl2(PPh3)2 (1.8 g, 2.8 mmol) were dissolved in 150 mL of Et2O. 3,5-Di-t-butylphenylmagnesium bromide (10 g, 37 mmol) as a Et2O solution was added to the solution 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 4.6 g (40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380121B1
Source datasetuspto-grants-2002_04
ORD IDord-31bddad286b64b4fa02ed3a05ddf8218
Source noteuspto-grants-2002_04