HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963126Generated: October 26, 2026
Ethanolamine → N-(2-Hydroxyethyl)maleimide
https://huagongshe.com/reaction/963126
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | N-(Methoxycarbonyl)maleimide | HCID 580610 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | N-(2-Hydroxyethyl)maleimide | HCID 458487 | 96.1% |
Reaction Steps
As shown in FIG. 1, to a solution of ethanolamine (1.8 g, 29.5 mmol) in saturated sodium bicarbonate solution (100 ml) was added N-methoxycarbonylmaleimide (95 g, 32.3 mmol) in portions with vigorous stirring at 0° C. The mixture was allowed to warm to room temperature and stirred for 1 hour. The pH of the mixture was adjusted to 6-7 by careful addition of concentrated sulfuric acid (5 ml). The resultant solution was freeze dried and the solid residue extracted with ethyl acetate (2×400 ml) by stirring for 30 min. with each extraction. The ethyl acetate extracts were collected by filtration and evaporated in vacuo to afford N-(2-hydroxyethyl)maleimide (formula I) as a white solid (4.0 g, 96% yield); thin layer chromatography (TLC), Rf=0.27, ethyl acetate/petroleum ether 1:1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05763196 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-de7500cbb7b04077815fb0593c79b098 |
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| Source note | uspto-grants-1998_06 |
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