HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359308Generated: October 25, 2026
Dimethylformamide → 2-Ethylhexyl 4-(3,4-dimethoxyphenylmethylene)-2,5-dioxo-1-imidazolidinepropionate
https://huagongshe.com/reaction/359308
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Ethylhexyl acrylate | HCID 7636 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-[(3,4-Dimethoxyphenyl)methylidene]imidazolidine-2,4-dione | HCID 165798 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Ethylhexyl 4-(3,4-dimethoxyphenylmethylene)-2,5-dioxo-1-imidazolidinepropionate | HCID 54409521 | 77.8% |
Reaction Steps
20 g (80.6 mmol) of 5-(3,4-dimethoxybenzylidene)-hydantoin, 17.8 g (96 mmol) of 2-ethylhexyl acrylate and 0.90 g (1.6 mmol) of potassium hydroxide were added to 150 ml of dimethylformamide, and the mixture was stirred at 110° C. for 2 hours. After cooling, the reaction solution was added with 200 ml of water and extracted with 500 ml of ethyl acetate. The extract was dried with sodium sulfate and then the solvent was distilled off under reduced pressure. The residue was recrystallized with toluene-n-hexane (1:1) and the precipitated crystals were dried to obtain 27.1 g of 2-ethylhexyl 4-(3,4-dimethoxyphenylmethylene)-2,5-dioxo-1-imidazolidinepropionate (yield: 77.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05000945 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-fe84fff7d4cd4b6ca592861b3f59b72a |
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| Source note | uspto-grants-1991_03 |
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