Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448128Generated: November 2, 2026

Acetic Acid → 3-Ethyl-N-methyl-5-(2-oxo-2-phenylethyl)-1,2-oxazole-4-carboxamide

https://huagongshe.com/reaction/1448128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-Ethyl-5-(2-hydroxy-2-phenylethyl)-N-methyl-1,2-oxazole-4-carboxamideHCID 20348838—
Catalystchromium (VI) trioxideHCID 10219390—
SolventWaterHCID 962—
Product3-Ethyl-N-methyl-5-(2-oxo-2-phenylethyl)-1,2-oxazole-4-carboxamideHCID 20382107—

Reaction Steps

A solution of 29.0 g. (0.105 mole) of 3-ethyl-5-(β-hydroxyphenethyl)-N-methyl-isoxazole-4-carboxamide and 500 ml. acetic acid at room temperature is treated dropwise rapidly with 12.5 g. (0.125 mole) of chromium trioxide in 125 ml. water. The resulting solution is stirred for 2 hours at room temperature and a portion of the acetic acid is removed in vacuo. The remainder is poured onto ice water and extracted with methylene chloride. The methylene chloride layer is washed with 2 N sodium hydroxide, dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo. The solid residue is triturated with ether and recrystallized from ethanol to give 3-ethyl-N-methyl-5-phenacyl-4-isoxazole carboxamide, m.p. 134° to 136° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179566
Source datasetuspto-grants-1979_12
ORD IDord-df820710575e48db8ca7fc6b01134ca0
Source noteuspto-grants-1979_12