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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1383749Erstellt: 24. Oktober 2026

Potassium Carbonate → Phosphoric Acid 2,5-dioxo-4,4-diphenyl-imidazolidin-1-ylmethyl Ester Dimethyl Ester

https://huagongshe.com/de/reaction/1383749

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt3-(Chloromethyl)-5,5-diphenylimidazolidine-2,4-dioneHCID 11098633—
EduktDimethyl phosphate, potassium saltHCID 23666574—
KatalysatorPotassium IodideHCID 4875—
LösungsmittelAcetonitrileHCID 6342—
ProduktPhosphoric Acid 2,5-dioxo-4,4-diphenyl-imidazolidin-1-ylmethyl Ester Dimethyl EsterHCID 1545954341,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Thirty grams of 3-(chloromethyl)-5,5-diphenyl-2,4-imidazolidinedione from Step (A), 17.1 g of potassium dimethyl phosphate, 0.6 g of potassium carbonate, and 0.15 g of potassium iodide were slurried into 75 mL of acetonitrile. The reaction mixture was heated at reflux for 3 hours. The solution was filtered to remove potassium chloride precipitate and concentrated to thick oil. Isopropyl alcohol was added to the oil and cooled to 0° C. The product was filtered and dried under vacuum. Sixteen grams of the title compound was obtained (40.9% yield); mp 123.1-124.3° C. Proton nuclear magnetic resonance spectroscopy (1H NMR) deuterated dimethyl sulfoxide (DMSO-d6): 3.6 ppm (d, 6H), 5.3 (d, 2H), 7.3-7.5 (m, 10H), 10.0 (s, 1H); doublets from long range phosphorous coupling.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06255492B1
Quelldatensatzuspto-grants-2001_07
ORD IDord-39384ed111e54056b81ed90d5be2440e
Quellennotizuspto-grants-2001_07