HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044761Generated: October 31, 2026
Nitrogen → Ethyl 2-acetyloxazole-4-carboxylate
https://huagongshe.com/reaction/1044761
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | (E)-ethyl 2-(1-phenylprop-1-en-2-yl)oxazole-4-carboxylate | HCID 66819964 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 2-acetyloxazole-4-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563714B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-bbe1bc029f3445519a6ae3d45a879f44 |
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| Source note | uspto-grants-2013_10 |
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