HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988263Generated: November 1, 2026
Potassium Cyanide → 5-(1-(Benzyloxycarbonylamino)-2-(3-tert-butyl-4-hydroxylphenyl)ethyl)imidazolidine-2,4-dione
https://huagongshe.com/reaction/1988263
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ammonium Carbonate | HCID 517111 | — |
| Reactant | Z-Tyr(3-tBu)-H | HCID 87606131 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(1-(Benzyloxycarbonylamino)-2-(3-tert-butyl-4-hydroxylphenyl)ethyl)imidazolidine-2,4-dione | HCID 17819196 | 53% |
Reaction Steps
To a solution of Z-Tyr(3-tBu)-H (2.18 g, 6.14 mmol) in ethanol (25 ml), potassium cyanide (480 mg, 7.37 mmol), 30% ammonium carbonate (1.77 g, 18.4 mmol) and water (25 ml) were added and stirred at 60° C. for 8 hours. The mixture was left for cooling and mixed with a saturated aqueous NaHCO3 solution. The organic layer was extracted with ethyl acetate and washed with water and then with saturated brine, dried over anhydrous magnesium sulfate and evaporated to remove the solvent under reduced pressure; the thus obtained residue was subjected to silica gel column chromatography (developing solvent: ethyl acetate:n-hexane=1:1), giving the titled compound (1.38 g, 53%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07553969B1 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-40279afe26a94e37b0d9304f545ce29d |
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| Source note | uspto-grants-2009_06 |
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