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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2384106Generated: November 2, 2026

1,4-Dioxane → Ethyl 5-hydroxy-1,2,4-oxadiazole-3-carboxylate

https://huagongshe.com/reaction/2384106

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 178472862HCID 178472862—
ProductEthyl 5-hydroxy-1,2,4-oxadiazole-3-carboxylateHCID 135973140—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of ethyl 2-(hydroxyamino)-2-iminoacetate (2 g, 15.14 mmol) in dioxane (15.00 mL) is added CDl (2.7 g, 16.65 mmol) and DBU (2.5 ml, 16.65 mmol) at room temperature. After stirring for 1 hour at 80° C., the reaction is quenched with 1N HCl, and the crude is diluted with EtOAc. The organic layer is washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to give ethyl 5-oxo-4,5-dihydro-1,2,4-oxadiazole-3-carboxylate (2.4 g). HPLC retention time=0.72 minutes (condition B); MS 159.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263629B2
Source datasetuspto-grants-2012_09
ORD IDord-ff9e2b1bb1f74f31a91ed12032b2f11a
Source noteuspto-grants-2012_09