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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746033Generated: November 1, 2026

Sulfuric Acid → 2-Tert-butyl-5-methyl-4-oxazoleacetic acid

https://huagongshe.com/reaction/746033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantMethyl 4-oxo-3-pivaloylaminovalerateHCID 13282913—
SolventAcetic AnhydrideHCID 7918—
Product2-Tert-butyl-5-methyl-4-oxazoleacetic acidHCID 13282973—

Reaction Conditions

Temperature80 °C

Reaction Steps

Methyl 4-oxo-3-pivaloylaminovalerate was dissolved in acetic anhydride (15 ml), and concentrated sulfuric acid (1.2 ml) was added dropwise with stirring. The mixture was allowed to stand at room temperature for 20 minutes and heated at 80° C. for 5 minutes. The acetic anhydride was distilled off under reduced pressure and the residue was poured into 50 ml of ice water. The mixture was neutralized with potassium carbonate and extracted with ethyl ether. The ethyl ether layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was then distilled off and the oily residue (2.5 g) was stirred in a mixture of ethanol (13 ml) and 2N sodium hydroxide (13 ml) at room temperature for 30 minutes. The reaction mixture was diluted with water, adjusted to pH 2 with hydrochloric acid and extracted with ethyl ether. The ethyl ether layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was treated with hexane to give 2-tert-butyl-5-methyl-4-oxazoleacetic acid as crystals; yield 1.50 g (60.2%). Recrystallization from isopropyl ether gave colorless prisms melting at 121°-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04602027
Source datasetuspto-grants-1986_07
ORD IDord-c42d34f2d8fe4551b10f11b4b6fe9f21
Source noteuspto-grants-1986_07