HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389873Generated: October 29, 2026
Potassium Cyanide → 4-(4-Fluorophenyl)-4-[(2-propenyloxy)methyl]imidazolidine-2,5-dione
https://huagongshe.com/reaction/389873
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Ammonium Carbonate | HCID 517111 | — |
| Reactant | Water ethanol | HCID 19096565 | — |
| Reactant | 1-(4-Fluorophenyl)-2-(2-propenyloxy)ethanone | HCID 62029481 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethylacetate heptane | HCID 21899848 | — |
| Product | 4-(4-Fluorophenyl)-4-[(2-propenyloxy)methyl]imidazolidine-2,5-dione | HCID 67131210 | — |
Reaction Steps
1.8 g of 1-(4-fluorophenyl)-2-(2-propenyloxy)ethanone obtained in Step 2, 1.21 g of potassium cyanide and 4.69 g of ammonium carbonate are heated to 55° C. for 2 hours in 50 mL of a 50/50 ethanol/water mixture. While heating the mixture at 55° C. 4.69 g of ammonium carbonate is added 3 times after 1 hour, 4 and 15 hours respectively. The reaction mixture is then diluted with water and extracted with ethyl acetate. The organic solution is dried over sodium sulfate and evaporated to provide the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383608B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-11df138a0bf345c6b9676abed955402f |
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| Source note | uspto-grants-2013_02 |
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