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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19524Generated: October 26, 2026

Ethyl 6-methoxy-1-oxo-3-phenyl-1H-indene-2-carboxylate → 1-hydroxy-6-methoxy-1-(3-methoxy-phenyl)-3-phenyl-1H-indene-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/19524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 6-methoxy-1-oxo-3-phenyl-1H-indene-2-carboxylateHCID 23249734—
ReactantHCID 178490745HCID 178490745—
SolventTetrahydrofuranHCID 8028—
Product1-hydroxy-6-methoxy-1-(3-methoxy-phenyl)-3-phenyl-1H-indene-2-carboxylic acid ethyl esterHCID 1152450790.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

6-Methoxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid ethyl ester (100 mg, 0.325 mmol) obtained in Example 1 was dissolved in THF and 1.5 equivalents of 3-methoxyphenylmagnesium bromide were added thereto, followed by stirring for 1 hr at 0° C. Then, the reaction mixture washed with saturated saline and extracted with ethyl acetate. The organic layer was separated, dried over anhydrous MgSO4, and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 122 mg of the titled compound (yield: 90.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745439B2
Source datasetuspto-grants-2010_06
ORD IDord-561fdd55bd744beb8d9bda76c4e9af68
Source noteuspto-grants-2010_06