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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl AcetateHCID 8857—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantMethyl isocyanoacetateHCID 547815—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 5-methyl-1,3-oxazole-4-carboxylateHCID 12627321—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04853027
Source datasetuspto-grants-1989_08
ORD IDord-1b002f6b27fa4215b539eb1f325e4971
Source noteuspto-grants-1989_08