HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58643Generated: October 29, 2026
Water → Ethyl 5-phenyl-1,2,4-oxadiazole-3-carboxylate
https://huagongshe.com/reaction/58643
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl 2-amino-2-(hydroxyimino)acetate | HCID 6785548 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 5-phenyl-1,2,4-oxadiazole-3-carboxylate | HCID 4295554 | — |
Reaction Steps
Benzoyl chloride (0.219 mL; 1.89 mmol) was added to a mixture of ethyl 2-amino-2-(hydroxyimino)acetate (0.250 g; 1.89 mmol) and N,N diisopropylethylamine (0.527 mL; 3.03 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 aqueous layer was extracted with dichloromethane, and the combined organic extracts were dried and concentrated under reduced pressure. The residue was refluxed in a sealed tube with pyridine (6 mL) for 20 hours 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 0.239 (60%) of ethyl 5-phenyl-1,2,4-oxadiazole-3-carboxylate as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434722B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-2f399569cc724f2ba52a69d284ce46d2 |
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| Source note | uspto-grants-2016_09 |
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