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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072723Generated: November 3, 2026

Hydrochloric Acid → (2R)-2-([4-[1-(4-Pentylphenylethyl)-5-methyl-1H-pyrrol-2-yl]phenyl]oxy)-3-phenylpropanoic acid

https://huagongshe.com/reaction/1072723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl (2R)-2-([4-[1-(4-pentylphenylethyl)-5-methyl-1H-pyrrol-2-yl]phenyl]oxy)-3-phenylpropanoateHCID 86588894—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product(2R)-2-([4-[1-(4-Pentylphenylethyl)-5-methyl-1H-pyrrol-2-yl]phenyl]oxy)-3-phenylpropanoic acidHCID 6973237198%

Reaction Steps

To a mixed solution of ethyl (2R)-2-([4-[1-(4-pentylphenylethyl)-5-methyl-1H-pyrrol-2-yl]phenyl]oxy)-3-phenylpropanoate (660 mg, 1.26 mmol) in THF (15 ml) and methanol (7 ml) was added 1N aqueous potassium hydroxide (4.0 ml, 4.0 mmol) and the mixture was stirred for 1 hour at room temperature. The reaction solution was neutralized with 1N hydrochloric acid, extracted with ethyl acetate, washed with saturated brine and dried over magnesium sulfate anhydride. The solvent was removed under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate) to give the object compound as an oily substance. 615 mg, (yield 98%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911468B2
Source datasetuspto-grants-2005_06
ORD IDord-009d94c5fd2846ee8d4fd1282978fca7
Source noteuspto-grants-2005_06