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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 3-(Chloromethyl)-5,5-diphenylimidazolidine-2,4-dione | HCID 11098633 | — |
| Edukt | Potassium di-tert-butyl phosphate | HCID 23674467 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | Phosphoric Acid di-tert-butyl Ester 2,5-dioxo-4,4-diphenyl-imidazolidin-1-ylmethyl Ester | HCID 15459545 | 38,6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06255492B1 |
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| Quelldatensatz | uspto-grants-2001_07 |
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| ORD ID | ord-92da913ed7284ceca65d24fa3ae26c6d |
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| Quellennotiz | uspto-grants-2001_07 |
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