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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049446Generated: October 31, 2026

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

https://huagongshe.com/reaction/1049446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 3-cyclopropyl-3-(3-(((2'-fluoro-5'-methoxy-3-(1-methoxy-3,3-dimethylbutyl)-[1,1'-biphenyl]-4-yl)oxy)methyl)phenyl)propanoateHCID 117760178—
SolventEthanolHCID 702—
Product3-Cyclopropyl-3-(3-(((2'-fluoro-5'-methoxy-3-(1-methoxy-3,3-dimethylbutyl)biphenyl-4-yl)oxy)methyl)phenyl)propanoic acidHCID 11776017168.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of ethyl 3-cyclopropyl-3-(3-(((2′-fluoro-5′-methoxy-3-(1-methoxy-3,3-dimethylbutyl)-[1,1′-biphenyl]-4-yl)oxy)methyl)phenyl)propanoate (385 mg) in ethanol (3.0 mL) was added 1N aqueous sodium hydroxide solution (3.0 mL), and the reaction mixture was stirred at 50° C. for 1 hr. 1N Hydrochloric acid was added, 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 (250 mg) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382188B2
Source datasetuspto-grants-2016_07
ORD IDord-a6a532d5f8be4e9685cbc1cb2c6f4814
Source noteuspto-grants-2016_07