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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918610Generated: October 25, 2026

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

https://huagongshe.com/reaction/1918610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-Fluorophenylacetic acidHCID 67617—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 2-amino-2-(hydroxyimino)acetateHCID 6785548—
CatalystDimethylformamideHCID 6228—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-(3-fluorobenzyl)-1,2,4-oxadiazole-3-carboxylateHCID 6337972230%

Reaction Steps

This compound was prepared according to general method 2 with (step I) 2-(3-fluorophenyl)acetic acid (1.03 g; 7.57 mmol) and oxalyl chloride (0.704 mL; 8.33 mmol) in dichloromethane (5 mL) and a few drops of DMF and (step II) ethyl 2-amino-2-(hydroxyimino)acetate (1.0 g; 7.57 mmol) and N,N diisopropylethylamine (2.11 mL; 12.11 mmol) in dichloromethane (10 mL) and (step 110 pyridine (18 mL). The crude material was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.555 g (30%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-6ec377ae5dea416391770000f7525d44
Source noteuspto-grants-2013_12