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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843551Generated: November 1, 2026

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

https://huagongshe.com/reaction/843551

Reaction equation

Participants

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

Reaction Steps

4-Chloro-2-methylindene (6.1 g, 37 mmol) and NiCl]2(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 numberUS06380120B1
Source datasetuspto-grants-2002_04
ORD IDord-139c96f7f2944029bcf69230d0008ea5
Source noteuspto-grants-2002_04