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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918632Generated: November 1, 2026

Water → Ethyl 5-phenyl-1,2,4-oxadiazole-3-carboxylate

https://huagongshe.com/reaction/1918632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzoyl chlorideHCID 7412—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 2-amino-2-(hydroxyimino)acetateHCID 6785548—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-phenyl-1,2,4-oxadiazole-3-carboxylateHCID 4295554—

Reaction Steps

Benzoyl chloride (0.219 mL; 1.89 mmol) was added to a mixture of ethyl 2-amino-2-(hydroxyimino)acetate (0.250 g; 1.89 mmol) and N,N diisopropylethylamine (0.527 mL; 3.03 mmol) in dichloromethane (18 mL) at −15° C. The reaction mixture was stirred at room temperature overnight and poured into a mixture of ice and water. The aqueous layer was extracted with dichloromethane, and the combined organic extracts were dried and concentrated under reduced pressure. The residue was refluxed in a sealed tube with pyridine (6 mL) for 20 hours and concentrated under reduced pressure. The crude material was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.239 (60%) of ethyl 5-phenyl-1,2,4-oxadiazole-3-carboxylate as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-46e807a60a9e4a8f873846e4c36920d0
Source noteuspto-grants-2013_12