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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 178472862 | HCID 178472862 | — |
| Product | Ethyl 5-hydroxy-1,2,4-oxadiazole-3-carboxylate | HCID 135973140 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263629B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-ff9e2b1bb1f74f31a91ed12032b2f11a |
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| Source note | uspto-grants-2012_09 |
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