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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918602Generated: October 27, 2026

Water → Ethyl 5-(3-Methoxybenzyl)-1,2,4-oxadiazole-3-carboxylate

https://huagongshe.com/reaction/1918602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Methoxyphenylacetyl chlorideHCID 2733246—
ReactantEthyl 2-amino-2-(hydroxyimino)acetateHCID 6785548—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-(3-Methoxybenzyl)-1,2,4-oxadiazole-3-carboxylateHCID 5106389215%

Reaction Steps

2-(3-methoxyphenyl)acetyl chloride (1.18 mL; 7.57 mmol) was added to a mixture of ethyl 2-amino-2-(hydroxyimino)acetate (0.500 g; 3.78 mmol) and N,N diisopropylethylamine (1.05 mL; 6.06 mmol) in dichloromethane (18 mL) at −15° C. The reaction mixture was stirred at room temperature overnight and poured into a mixture of ice and water. The formed precipitate was filtered off, suspended in pyridine (18 mL) and refluxed in a sealed tube for 20 h and concentrated under reduced pressure. The crude material was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.146 g (15%) of ethyl 5-(3-methoxybenzyl)-1,2,4-oxadiazole-3-carboxylate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-7b1c32cec1ed442c8d5e89aebcbf0b8a
Source noteuspto-grants-2013_12