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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475182Generated: November 1, 2026

Pyridine → Ethyl 3-[4-(trifluoromethoxy)phenyl]-1,2,4-oxadiazole-5-carboxylate

https://huagongshe.com/reaction/1475182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthoxalyl chlorideHCID 20884—
Reactantn-Hydroxy-4-trifluoromethoxy-benzamidineHCID 5702530—
SolventChloroformHCID 6212—
ProductEthyl 3-[4-(trifluoromethoxy)phenyl]-1,2,4-oxadiazole-5-carboxylateHCID 86711474109.5%

Reaction Steps

To a solution of (E)-N′-hydroxy-4-(trifluoromethoxy)benzimidamide (3.0 g, 13.6 mmol) and pyridine (1.6 g, 20.4 mmol) in CHCl3 (20 mL), ethyl 2-chloro-2-oxoacetate (2.2 g, 16.4 mmol) was added slowly at 0° C. The mixture was stirred at reflux for 3 h, and then concentrated to give the crude product, which was purified by silica gel column chromatography (Petroleum ether:EtOAc=10:1) to give ethyl 3-(4-(trifluoromethoxy)phenyl)-1,2,4-oxadiazole-5-carboxylate as a white solid (4.5 g, 82%). MS (ES+) C12H9F3N2O4 requires: 302. found: 303[M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018380B2
Source datasetuspto-grants-2015_04
ORD IDord-757374f7c79247dcae4e2adbe992e874
Source noteuspto-grants-2015_04