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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251525Generated: November 3, 2026

4-Chloro-2-(propan-2-yl)-1H-indene → HCID 18386460, compound

https://huagongshe.com/reaction/1251525

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-(propan-2-yl)-1H-indeneHCID 21918397—
ReactantHCID 178424303HCID 178424303—
CatalystHCID 178418751HCID 178418751—
SolventDiethyl EtherHCID 3283—
ProductHCID 18386460HCID 18386460—

Reaction Steps

4-Chloro-2-isopropylindene (9.8 g, 51 mmol) and NiCl2(PPh3)2 (1.8 g, 2.8 mmol) are dissolved in 150 mL of Et2O. 2-Methylphenylmagnesium bromide (51 mmol) as an Et20 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) and 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 6.6 g (52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342566B2
Source datasetuspto-grants-2002_01
ORD IDord-7e89a8e94dfa41aaaabd0d3399546456
Source noteuspto-grants-2002_01