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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044761Generated: October 31, 2026

Nitrogen → Ethyl 2-acetyloxazole-4-carboxylate

https://huagongshe.com/reaction/1044761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantWaterHCID 962—
Reactant(E)-ethyl 2-(1-phenylprop-1-en-2-yl)oxazole-4-carboxylateHCID 66819964—
SolventAcetoneHCID 180—
ProductEthyl 2-acetyloxazole-4-carboxylateHCID 66820192—

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of NaIO4 (23 g, 108 mmol) in water (150 mL) was slowly added to a vigorously stirred suspension of silica gel (110 g) in acetone (500 mL). The mixture was then concentrated under reduced pressure and the lumpy solid slurried in CH2Cl2 and the solvent was evaporated under reduced pressure. CH2Cl2 (500 mL) was added and the reaction mixture was treated at rt with (E)-2-(1-phenylprop-1-en-2-yl)oxazole-4-carboxylic acid ethyl ester (8.3 g, 32 mmol) and RuCl3 hydrate (1.1 g, 2 mmol). The reaction mixture was stirred at rt in the dark for 60 min, filtered and concentrated under reduced pressure. Purification of the residue by FC (1:0 to 1:5 petroleum ether-Et2O) gave the title compound as a pale yellow solid. TLC:rf (1:1 EA-Hept)=0.52. LC-MS-conditions 01: tR=0.70 min; [M+H]+=183.99.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563714B2
Source datasetuspto-grants-2013_10
ORD IDord-bbe1bc029f3445519a6ae3d45a879f44
Source noteuspto-grants-2013_10