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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70896Generated: October 25, 2026

1,1'-Carbonyldiimidazole → ethyl 5-hydroxy-1,2,4-oxadiazole-3-carboxylate

https://huagongshe.com/reaction/70896

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 178472862HCID 178472862—
Solvent1,4-DioxaneHCID 31275—
Productethyl 5-hydroxy-1,2,4-oxadiazole-3-carboxylateHCID 135973140100.3%

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 CDI (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 D); MS 159.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822534B2
Source datasetuspto-grants-2014_09
ORD IDord-19daf404387445e0bc0f718819b306ac
Source noteuspto-grants-2014_09