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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294289Generated: November 4, 2026

Hydrochloric Acid → 2-[3-[2-[(5-Methyl-2-phenyl-4-oxazolyl)methoxy]-4-pyridylmethoxy]phenyl]acetic acid

https://huagongshe.com/reaction/1294289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-[3-[2-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]-4-pyridylmethoxy]phenyl]acetateHCID 68886931—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-[3-[2-[(5-Methyl-2-phenyl-4-oxazolyl)methoxy]-4-pyridylmethoxy]phenyl]acetic acidHCID 68884379—

Reaction Steps

To a mixture of methyl 2-[3-[2-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]-4-pyridylmethoxy]phenyl]acetate (0.596 g), tetrahydrofuran (6.0 mL) and methanol (6.0 mL) was added a 1N aqueous sodium hydroxide solution (3.0 mL), and the mixture was stirred at room temperature for 1 hr. 1N Hydrochloric acid (3.0 mL) and water were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated to give crystals of 2-[3-[2-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]-4-pyridylmethoxy]phenyl]acetic acid. Recrystallization from ethanol-hexane gave colorless prism crystals (0.566 g, 98%). melting point: 148-149° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238716B2
Source datasetuspto-grants-2007_07
ORD IDord-df87fa4524c24484ad2a194a263bfffb
Source noteuspto-grants-2007_07