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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945073Generated: October 31, 2026

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

https://huagongshe.com/reaction/1945073

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 numberUS08394853B2
Source datasetuspto-grants-2013_03
ORD IDord-b8ec2aed101140fc8df21518ea02c7eb
Source noteuspto-grants-2013_03