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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650396Generated: October 28, 2026

Ethyl 3-(3,4-methylenedioxyphenyl)1-oxoindene-2-carboxylate → 1-(4-Fluorophenyl)-3-(3,4-methylenedioxyphenyl)indane-2-carboxylic acid

https://huagongshe.com/reaction/650396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(3,4-methylenedioxyphenyl)1-oxoindene-2-carboxylateHCID 18427631—
ReactantEthyl (1RS)-1-(4-Fluorophenyl)-1-hydroxy-3-(3,4-methylenedioxyphenyl)indene-2-carboxylateHCID 18969656—
ReactantHCID 178418676HCID 178418676—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Fluorophenyl)-3-(3,4-methylenedioxyphenyl)indane-2-carboxylic acidHCID 1590850135%

Reaction Steps

Ethyl (1RS)-1-(4-Fluorophenyl)-1-hydroxy-3-(3,4-methylenedioxyphenyl)indene-2-carboxylate. To a solution of ethyl 3-(3,4-methylenedioxyphenyl)-1-oxoindene-2-carboxylate (100 mg, 0.31 mmol) in THF (5 ml) under an argon atmosphere at 0° C. was added a solution of freshly prepared 4-fluorophenyl magnesium bromide (0.62 mmol). After stirring for 45 min, the mixture was partitioned between 3M HCl and EtOAc. The organic extract was washed successively with H2O, 5% aqueous NaHCO3 and saturated aqueous NaCl. The solvent was removed in vacuo, and the residue was purified by flash chromatography, eluting with 15% EtOAc/hexanes to afford the title compound (45 mg, 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06271399B1
Source datasetuspto-grants-2001_08
ORD IDord-7e8d00299c8147abb583f19b6c704213
Source noteuspto-grants-2001_08