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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399205Generated: October 27, 2026

4-Bromoanisole → Ethyl(1RS)-1-Hydroxy-1-(4-methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indene-2-carboxylate

https://huagongshe.com/reaction/399205

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanisoleHCID 7730—
ReactantMagnesiumHCID 5462224—
ReactantEthyl 3-(3,4-methylenedioxyphenyl)1-oxoindene-2-carboxylateHCID 18427631—
ReactantHCID 178491912HCID 178491912—
SolventEther tetrahydrofuranHCID 21868444—
ProductEthyl(1RS)-1-Hydroxy-1-(4-methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indene-2-carboxylateHCID 1896964580%

Reaction Steps

A solution of 4-bromoanisole (0.89 g, 5.0 mmol) in 9:1 Et2O/THF (10 ml) was added to magnesium turnings (0.105 g, 5.0 mmol), and the resulting mixture was allowed to stir for 30 min. The resultant 4-methoxyphenyl magnesium bromide was added dropwise to a solution of ethyl 3-(3,4-methylenedioxyphenyl)-1-oxoindene-2-carboxylate (0.77 g, 2.4 mmol) in 10:1 Et2O/THF (55 ml) at 0° C. The resulting mixture was stirred at 0° C. for 1 h and was then partitioned between EtOAc and 1M HCl. The aqueous phase was extracted with EtOAc, and the combined organic extracts were washed successively with 5% aqueous NaHCO3 and saturated aqueous NaCl and dried (MgSO4). The solvent was removed under reduced pressure, and the residue was purified by flash chromatography on silica gel, eluting with 10% EtOAc/hexanes to afford the title compound as a yellow glassy solid (0.80 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05817693
Source datasetuspto-grants-1998_10
ORD IDord-390a0df80572477b81bfbb7effca0647
Source noteuspto-grants-1998_10