HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032075Generated: October 31, 2026
Water → Ethyl [(2-methylacryloyl)amino](oxo)acetate
https://huagongshe.com/reaction/1032075
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methacrylamide | HCID 6595 | — |
| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl [(2-methylacryloyl)amino](oxo)acetate | HCID 14298183 | 31.8% |
Reaction Steps
Into the same reaction vessel as used in Example 1, ethoxalyl chloride (12.3 g; 0.09 mol) was charged, and the reaction vessel was cooled in an ice bath. A solution of methacrylamide (7.7 g; 0.09 mol) in chloroform (32.4 ml) was dropwise added thereto in 10 minutes. After completion of the addition, a mixture of pyridine (7.2 g; 0.09 mol) and chloroform (10 ml) was added thereto, and the resulting mixture was stirred at room temperature for 1 hour. The reaction mixture was shaken with chloroform (500 ml) and water (500 ml), and the chloroform layer was separated and dried over anhydrous magnesium sulfate, followed by removal of chloroform. Hydroquinone (0.01 g) was added thereto, and distillation under reduced pressure was carried out to give N-ethoxalylmethacrylamide (5.3 g). Yield, 32%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04956491 |
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| Source dataset | uspto-grants-1990_09 |
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| ORD ID | ord-994b90a12a7940ceb0618543f19beac2 |
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| Source note | uspto-grants-1990_09 |
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