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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918595Generated: October 25, 2026

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

https://huagongshe.com/reaction/1918595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-(Trifluoromethyl)benzeneacetic acidHCID 67695—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 2-amino-2-(hydroxyimino)acetateHCID 6785548—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-(3-(trifluoromethyl)benzyl)-1,2,4-oxadiazole-3-carboxylateHCID 668321614%

Reaction Steps

This compound was prepared according to general method 2 with (step I) 2-(3-(trifluoromethyl)phenyl)acetic acid (0.773 g; 3.78 mmol) and oxalyl chloride (0.352 mL; 4.16 mmol) in dichloromethane (12 mL) with few drops of DMF and (step II) ethyl 2-amino-2-(hydroxyimino)acetate (0.5 g; 3.78 mmol) and N,N diisopropylethylamine (1.05 mL; 6.06 mmol) in dichloromethane (6 mL) and (step III) pyridine (18 mL). The crude material was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.040 g (4%) of ethyl 5-(3-(trifluoromethyl)benzyl)-1,2,4-oxadiazole-3-carboxylate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-cb7419ae08fb45b59b2cba58c1f74fc8
Source noteuspto-grants-2013_12