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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58598Generated: October 26, 2026

3-Thiophenacetic acid → Ethyl 5-[(thiophen-3-yl)methyl]-1,2,4-oxadiazole-3-carboxylate

https://huagongshe.com/reaction/58598

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Thiophenacetic acidHCID 23404—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 2-amino-2-(hydroxyimino)acetateHCID 6785548—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-[(thiophen-3-yl)methyl]-1,2,4-oxadiazole-3-carboxylateHCID 6338266638.1%

Reaction Steps

This compound was prepared according to general method 2 with (step I) 2-(thiophen-3-yl)acetic acid (0.568 g; 3.78 mmol), oxalyl chloride (0.352 mL; 4.16 mmol) in dichloromethane (12 mL) with few drops of DMF; (step II) ethyl 2-amino-2-(hydroxyimino)acetate (0.5 g; 3.78 mmol); 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 0.343 g (38%) of ethyl 5-(thiophen-3-ylmethyl)-1,2,4-oxadiazole-3-carboxylate as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434722B2
Source datasetuspto-grants-2016_09
ORD IDord-5b7e18e865d74e309b3da04ad4b2be92
Source noteuspto-grants-2016_09