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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58619Generated: October 26, 2026

Water → Ethyl 5-(4-fluorobenzyl)-1,2,4-oxadiazole-3-carboxylate

https://huagongshe.com/reaction/58619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Fluorophenylacetyl chlorideHCID 3744988—
ReactantEthyl 2-amino-2-(hydroxyimino)acetateHCID 6785548—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-(4-fluorobenzyl)-1,2,4-oxadiazole-3-carboxylateHCID 5518527233.3%

Reaction Steps

2-(4-fluorophenyl)acetyl chloride (0.518 mL; 3.78 mmol) was added to a mixture of ethyl 2-amino-2-(hydroxyimino)acetate (0.5 g; 3.78 mmol) and N,N diisopropylethylamine (1.05 mL; 6.06 mmol) in dichloromethane (15 mL) at −15° C. The reaction mixture was stirred at room temperature overnight and poured into a mixture of ice and water. The formed precipitate was filtered off, suspended in pyridine (18 mL) and refluxed in a sealed tube for 20 h 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 0.315 g (33%) of ethyl 5-(4-fluorobenzyl)-1,2,4-oxadiazole-3-carboxylate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434722B2
Source datasetuspto-grants-2016_09
ORD IDord-8363eb0f840b4fff87518327be7743b0
Source noteuspto-grants-2016_09