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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664578Generated: November 1, 2026

Hydrochloric Acid → 4-(3-Phenyl-1,2,4-oxadiazol-5-yl)butanoic acid

https://huagongshe.com/reaction/1664578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 3-(3-phenyl-1,2,4-oxadiazol-5-yl)butanoateHCID 66725791—
Product4-(3-Phenyl-1,2,4-oxadiazol-5-yl)butanoic acidHCID 66725299%

Reaction Steps

To a solution of methyl 3-(3-phenyl-1,2,4-oxadiazol-5-yl)butanoate (1.53 g, 6.21 mmole) in methanol (10 ml) was added 1N NaOH (10 mL). After stirring at room temperature for 2 hours, the reaction solution was acidified to pH=3-4 with 6N HCl under an ice bath and then extracted with ethyl acetate three times. The combined organic layers were washed with water and then brine, dried over Na2SO4, filtered and concentrated to give the desired product (1.44 g, 99% yield) as white solid. LCMS calculated for C12H13N2O3 (M+H): 233.1. found: 233.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039478B2
Source datasetuspto-grants-2011_10
ORD IDord-ecb27b52df78403ca9f76324548b1b7d
Source noteuspto-grants-2011_10