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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantSodium BicarbonateHCID 516892—
ReactantAmmonium CarbonateHCID 517111—
ReactantZ-Tyr(3-tBu)-HHCID 87606131—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product5-(1-(Benzyloxycarbonylamino)-2-(3-tert-butyl-4-hydroxylphenyl)ethyl)imidazolidine-2,4-dioneHCID 1781919653%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553969B1
Source datasetuspto-grants-2009_06
ORD IDord-40279afe26a94e37b0d9304f545ce29d
Source noteuspto-grants-2009_06