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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049453Generated: November 4, 2026

Hydrochloric Acid → 3-Cyclopropyl-3-(3-(((2-fluoro-5-methoxy-4''-(trifluoromethyl)-1,1':2',1''-terphenyl-4'-yl)oxy)methyl)phenyl)propanoic acid

https://huagongshe.com/reaction/1049453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 3-cyclopropyl-3-(3-(((2-fluoro-5-methoxy-4''-(trifluoromethyl)-1,1':2',1''-terphenyl-4'-yl)oxy)methyl)phenyl)propanoateHCID 117760114—
SolventEthanolHCID 702—
Product3-Cyclopropyl-3-(3-(((2-fluoro-5-methoxy-4''-(trifluoromethyl)-1,1':2',1''-terphenyl-4'-yl)oxy)methyl)phenyl)propanoic acidHCID 11776003697%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of ethyl 3-cyclopropyl-3-(3-(((2-fluoro-5-methoxy-4″-(trifluoromethyl)-1,1′:2′,1″-terphenyl-4′-yl)oxy)methyl)phenyl)propanoate (92 mg) in ethanol (3.0 mL) was added 2N aqueous sodium hydroxide solution (0.16 mL), and the mixture was stirred at 50° C. for 15 hr. To the reaction mixture was added 1N hydrochloric acid, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (85 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382188B2
Source datasetuspto-grants-2016_07
ORD IDord-442ccd267e954df8bd82a3155e4ecb1f
Source noteuspto-grants-2016_07