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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716435Generated: November 1, 2026

Hydrochloric Acid → 4-Methyl-1,3-oxazole-5-carboxylic acid

https://huagongshe.com/reaction/1716435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormamideHCID 713—
ReactantEthyl 2-chloroacetoacetateHCID 11858—
ReactantSodium HydroxideHCID 14798—
SolventEthyl AcetateHCID 8857—
Product4-Methyl-1,3-oxazole-5-carboxylic acidHCID 29231164.5%

Reaction Conditions

Temperature120 °C

Reaction Steps

Ethyl-2-chloroacetoacetate (1 wt; 1 eq., 1000 g) was aged with formamide (0.68 vol; ca. 2.8 eq.) and the resulting solution was heated to 120° C. After 5 hours the mixture was allowed to cool to room temperature and allowed to age under nitrogen over night. The mixture was treated with NaOH (3 M, 6 vol, reaction moderately exothermic) and stirred at room temperature for 4 hours. Ethyl acetate (6 vol) was added and the phases allowed to separae. The organic layer was discarded while the aqueous was acidified with conc. (32%) aqueous HCl to pH 2 (ca. 2.0 vol). A precipitate started to form. The suspension was treated with AcOEt (8 vol) and vigorously stirred until the bulk of the precipitate had dissolved. The aqueous phase was further extracted with AcOEt twice (6 vol each) and the combined organic layers distilled to low volume (again a suspension was observed at low volume). Fresh AcOEt (8 vol) was added and the mixture evaporated to dryness. The collected solid was placed in the oven at 40° C. over night under reduced pressure to give 4-methyl-1,3-oxazole-5-carboxylic acid (498 g, 64.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803820B2
Source datasetuspto-grants-2010_09
ORD IDord-e382089fd80640448b4366d18e8fe8ff
Source noteuspto-grants-2010_09