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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040050Generated: November 1, 2026

Nitrogen → Ethyl 2-acetyloxazole-4-carboxylate

https://huagongshe.com/reaction/2040050

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 NalO4 (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)-ethyl 2-(1-phenylprop-1-en-2-yl)oxazole-4-carboxylate (8.3 g, 32.5 mmol) and RuC1-3 hydrate (550 mg, 1.0 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→1:5 petroleum ether: Et2O) gave the title compound as a yellow solid. TLC:rf (1:1 EA-Hept)=0.52.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580831B2
Source datasetuspto-grants-2013_11
ORD IDord-63ad028ee87b4fc1b6c5b99fc9e89d3e
Source noteuspto-grants-2013_11