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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918599Generated: October 26, 2026

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

https://huagongshe.com/reaction/1918599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactantp-Tolylacetic acidHCID 248474—
ReactantEthyl 2-amino-2-(hydroxyimino)acetateHCID 6785548—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-(4-methylbenzyl)-1,2,4-oxadiazole-3-carboxylateHCID 6338289623%

Reaction Steps

This compound was prepared according to general method 2 with (step I) 2-p-tolylacetic acid (0.568 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 (12 mL). The crude material was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.2118 g (23%) of ethyl 5-(4-methylbenzyl)-1,2,4-oxadiazole-3-carboxylate as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-854ce43ccc1f430f9d7edfa82f63060d
Source noteuspto-grants-2013_12