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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934774Generated: November 1, 2026

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

https://huagongshe.com/reaction/1934774

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 (1.8g, 2.8 mmol) are dissolved in 150 mL of Et2O. 2-Methylphenylmagnesium bromide (51 mmol) as an 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) 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 numberUS06384142B1
Source datasetuspto-grants-2002_05
ORD IDord-8019e3eccb104b98b6545ba53fadcb73
Source noteuspto-grants-2002_05