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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383750Generated: October 26, 2026

Potassium Iodide → Phosphoric Acid di-tert-butyl Ester 2,5-dioxo-4,4-diphenyl-imidazolidin-1-ylmethyl Ester

https://huagongshe.com/reaction/1383750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Chloromethyl)-5,5-diphenylimidazolidine-2,4-dioneHCID 11098633—
ReactantPotassium di-tert-butyl phosphateHCID 23674467—
SolventAcetonitrileHCID 6342—
ProductPhosphoric Acid di-tert-butyl Ester 2,5-dioxo-4,4-diphenyl-imidazolidin-1-ylmethyl EsterHCID 1545954538.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

35.5 Grams of 3-(chloromethyl)-5,5-diphenyl-2,4-imidazolidinedione from Step (A), 30.7 g of potassium di(t-butyl) phosphate, 0.6 g of potassium carbonate, and 0.15 g of potassium iodide were slurried into 200 mL acetonitrile. The reaction mixture was heated at reflux for 2.5 hours. The solution was filtered to remove potassium chloride precipitate. The filtrate was cooled to 0° C. and filtered to give 22.3 g of the title compound (38.6% yield); mp 108.5° C. (d). 1H NMR (DMSO-d6): 1.3 ppm (s, 18H), 5.2 (d, 2H), 7.3-7.5 (m, 10H), 9.9 (s, 1H); doublet from long range phosphorus coupling.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255492B1
Source datasetuspto-grants-2001_07
ORD IDord-92da913ed7284ceca65d24fa3ae26c6d
Source noteuspto-grants-2001_07