Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Reactant | HCID 66618606 | HCID 66618606 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 66681061 | HCID 66681061 | — |
Reaction Steps
1.8 g (22.2 mmol, 2 eq.) of potassium cyanate are added at 30° C. to a solution of 3.7 g (11.3 mmol, 1 eq.) of 1-(4-iodophenylamino)cyclohexanecarbonitrile in 30 ml of glacial acetic acid. The reaction medium is stirred at 60° C. overnight. 5 ml of hydrochloric acid and then 3 ml of water are added. The medium is heated at 90° C. for 1 hour and then at room temperature for 3 hours. Water is then poured into the reaction medium, and the precipitate formed is filtered off and then chromatographed on silica gel (50/50 heptane/ethyl acetate). 180 mg of 1-(4-iodophenyl)-1,3-diaza-spiro[4.5]decane-2,4-dione are obtained in the form of an orange-coloured solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420682B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-f85e1becdb1641de82cca07c27ceff52 |
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| Source note | uspto-grants-2013_04 |
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