HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073660Generated: October 26, 2026
Ethanol → Ethyl [(2-methylacryloyl)amino](oxo)acetate
https://huagongshe.com/reaction/1073660
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Isopropenyloxazoline-4,5-dione hydrochloride | HCID 22157615 | — |
| Product | Ethyl [(2-methylacryloyl)amino](oxo)acetate | HCID 14298183 | — |
Reaction Steps
In the same reaction vessel as used in Example 1, ethanol (230.4 g; 5.0 mol) and pyridine (39.6 g; 0.5 mol) were charged, and the reaction vessel was cooled at 0° C. in an ice bath. 2-Isopropenyloxazoline-4,5-dione hydrochloride (87.8 g; 0.5 mol) was added thereto in 30 minutes under stirring while keeping the reaction temperature at 0° to 10° C. After completion of the addition, excess ethanol was removed under reduced pressure. The reaction mixture was shaken with ethyl acetate (1,000 ml) and a large amount of water, and the ethyl acetate layer was separated and dried over anhydrous magnesium sulfate, followed by removal of ethyl acetate. Hydroquinone (0.01 g) was added thereto, and distillation under reduced pressure was carried out to give N-ethoxalylmethacrylamide (30.5 g). Yield, 33%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04970281 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-3fe0d2369b574c959423fdb0c9ad67bf |
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| Source note | uspto-grants-1990_11 |
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