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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1383750Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1383750

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktPotassium CarbonateHCID 11430—
Edukt3-(Chloromethyl)-5,5-diphenylimidazolidine-2,4-dioneHCID 11098633—
EduktPotassium di-tert-butyl phosphateHCID 23674467—
LösungsmittelAcetonitrileHCID 6342—
ProduktPhosphoric Acid di-tert-butyl Ester 2,5-dioxo-4,4-diphenyl-imidazolidin-1-ylmethyl EsterHCID 1545954538,6%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06255492B1
Quelldatensatzuspto-grants-2001_07
ORD IDord-92da913ed7284ceca65d24fa3ae26c6d
Quellennotizuspto-grants-2001_07