HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721815Generated: October 29, 2026
Acetic Anhydride → Methyl 5-methyl-1,3-oxazole-4-carboxylate
https://huagongshe.com/reaction/1721815
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Methyl isocyanoacetate | HCID 547815 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 5-methyl-1,3-oxazole-4-carboxylate | HCID 12627321 | — |
Reaction Steps
A stirred mixture of 10.0 g of methyl isocyanoacetate, 15.1 g of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) and 133 ml of anhydrous THF was cooled to 0° C., and a solution of 10.2 g of acetic anhydride in 33 ml of THF was added dropwise over 15 minutes. The mixture was stirred overnight at room temperature and stripped of solvent. The residue was mixed with 250 ml of ethyl acetate, the mixture was washed with water, dried (MgSO4), filtered and stripped of solvent. The residue was chromatographed on silica gel with a 1:1 v:v ethyl acetate/hexane mixture as eluent. The middle fractions gave methyl 5-methyl-4-oxazolecarboxylate (4A) as a white solid, m.p.: 46.5°-47.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04853027 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-1b002f6b27fa4215b539eb1f325e4971 |
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| Source note | uspto-grants-1989_08 |
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