HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624219Generated: October 26, 2026
Acetamide → Ethyl 2,4-dimethyl-1,3-oxazole-5-carboxylate
https://huagongshe.com/reaction/1624219
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetamide | HCID 178 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl 4-chloroacetoacetate | HCID 69484 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethyl 2,4-dimethyl-1,3-oxazole-5-carboxylate | HCID 315151 | — |
Reaction Steps
800 mmol of acetoamide and 400 mmol of ethylchloroaceto acetate were dissolved into 146 g of anhydrous acetic acid. Reaction was carried out for 10 hours at 130° C. The reacted liquid was alkalized with saturated sodium hydrogen carbonate and then the product was extracted into an organic phase using ethyl acetate. The organic phase was dried under sodium sulfate and then the solvent was evaporated out, obtaining a black liquid. To this black liquid 6N hydrochloric acid aqueous solution was added to make it alkaline. Then the product was extracted into organic phase using ethyl acetate. The thus obtained solid substance was dissolved in hexane. Insoluble matter was eliminated and solvent was evaporated out, obtaining ethyl 2,4-dimethyl-1,3-oxazole-5-carboxylate, an yellowish white solid (yield: 30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08779086B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-bfe287ac4b3b45a5ae023297950183de |
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| Source note | uspto-grants-2014_07 |
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