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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377025Generated: 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/377025

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 numberUS06022975
Source datasetuspto-grants-2000_02
ORD IDord-f7bcfff19c1a4986ad40630688605a06
Source noteuspto-grants-2000_02