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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11967Generated: October 25, 2026

Chloride → 2-(4-Fluorophenylmethyl)indene

https://huagongshe.com/reaction/11967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
Reactant4-Fluorobenzyl chlorideHCID 9602—
Reactant1H-Indene, 2-bromo-HCID 575586—
ReactantMagnesiumHCID 5462224—
CatalystHCID 178418745HCID 178418745—
SolventDiethyl EtherHCID 3283—
Product2-(4-Fluorophenylmethyl)indeneHCID 21976997—

Reaction Steps

To a suspension of freshly ground magnesium (0.58 g, 23 mmol) in 100 mL of ether was added about 3 mL of a 15 mL ether solution containing 3.0 g (21 mmol) of 4-fluorophenylmethyl chloride. The system was carefully heated and after initiation of the reaction, the remaining chloride solution added over 30 minutes while maintain a gentle reflux. After refluxing for 1.5 hours, the Grignard solution was cooled and cannulated to a mixture of 3.65 g (19 mmol) of 2-bromo-indene, 150 mg (0.20 mmol) of NiCl2(dppp) and 100 mL of ether. The system was gently heated to reflux overnight and then cooled and quenched by adding 150 mL of 1.0 M aqueous hydrochloric acid. The product was isolated and purified (hexanes/silica) as for 2-benzyl-indene. Yield: 3.45 g, 74 percent

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098356B2
Source datasetuspto-grants-2006_08
ORD IDord-c95ea336c63e4d4ea8961bed6584d030
Source noteuspto-grants-2006_08