Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Ammonium Carbonate | HCID 517111 | — |
| Reactant | HCID 23462695 | HCID 23462695 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21328251 | HCID 21328251 | — |
Reaction Steps
A suspension of 829 grams (3 moles) of diethyl 3-oxo-1,5,5-trimethylcyclohexylphosphonate (A. N. Pudovik and I. V. Konovalova, Zh, Obshch. Khim., 27, 1617 (1957), 293 grams (4.5 moles) of potassium cyanide, and 864 grams (9 moles) of powdered ammonium carbonate in 1200 ml of ethanol and 900 ml of water, was heated to 55° C. with stirring over a period of 30 minutes. The mixture was heated at 55° C. for an additional 5.5 hours, cooled to room temperature and filtered through a Buchner funnel. The resulting two diastereomeric hydantoin derivatives (isomers A and B) which differ in solubilities and melting points were then isolated, respectively, from the filter cake and filtrate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04145510 |
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| Source dataset | uspto-grants-1979_03 |
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| ORD ID | ord-c2716627df7843fbada9c45a7a826be7 |
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| Source note | uspto-grants-1979_03 |
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