Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 4-Acetylpyridine | HCID 14282 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Product | 5-Methyl-5-(4-pyridyl)hydantoin | HCID 222702 | — |
Reaction Steps
A mixture of 4-acetyl pyridine (3.0 mL), NH4HCO3 (7.73 g), KCN (2.16 g), and concentrated NH4OH (8.2 mL) in EtOH (10.35 mL) was heated to 60° C. overnight under a reflux condenser. The reaction mixture was extracted with ether, then acidified to pH 4.5 with concentrated HCl and extracted with EtOAc. The combined organic extracts from the acidic extraction were dried over Na2SO4. Solvent was removed in vacuo to yield crude 5-methyl-5-(4-pyridyl)-imidazolidinedione as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07125865B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-340defd244444dcfac925803ca7035ad |
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| Source note | uspto-grants-2006_10 |
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