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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163322Generated: October 28, 2026

Citric Acid → {5-[(2',6'-dimethylbiphenyl-3-yl)methoxy]-1H-indol-1-yl}acetic acid

https://huagongshe.com/reaction/1163322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantMethanolHCID 887—
ReactantPotassium HydroxideHCID 14797—
Reactantethyl {5-[(2',6'-dimethylbiphenyl-3-yl)methoxy]-1H-indol-1-yl}acetateHCID 58755253—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product{5-[(2',6'-dimethylbiphenyl-3-yl)methoxy]-1H-indol-1-yl}acetic acidHCID 2311176476%

Reaction Steps

To a solution of ethyl {5-[(2′,6′-dimethylbiphenyl-3-yl)methoxy]-1H-indol-1-yl}acetate (0.27 g, 0.65 mmol) in a mixed solvent of methanol (10 mL) and tetrahydrofuran (10 mL) was added 85% aqueous solution (5 mL) of potassium hydroxide (0.13 g, 1.97 mmol), and the mixture was stirred at room temperature for 18 hr. Water was added to the reaction mixture, and the mixture was made weak acidic with 10% aqueous citric acid solution and extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:2-2:1) to give the title compound (0.19 g, yield 76%) as a pale-yellow amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820837B2
Source datasetuspto-grants-2010_10
ORD IDord-fab6029b66e8438397929305197e182f
Source noteuspto-grants-2010_10