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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1033113Erstellt: 24. Oktober 2026

Chloromethyl Methyl Ether → Diethyl 1-(methoxymethyl)-2,5-dioxo-4-imidazolylphosphonate

https://huagongshe.com/de/reaction/1033113

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloromethyl Methyl EtherHCID 7864—
EduktSodium hydrideHCID 24758—
EduktDiethyl (2,5-dioxo-2,5-dihydro-1H-imidazol-4-yl)phosphonateHCID 53733419—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktDiethyl 1-(methoxymethyl)-2,5-dioxo-4-imidazolylphosphonateHCID 53791991—

Reaktionsschritte

To a solution of diethyl 2,5-dioxo-4-imidazolylphosphonate (3.61 g, 0.015 moles) in DMF (10 mL), under N2, is added sodium hydride (80% dispersion in oil) (0.55 g, 0.018 moles) and stirred for 5 minutes. Chloromethyl methyl ether (tech. grade 85%) (1.9 mL, 0.021 moles) is added. This mixture is stirred at room temperature for 4 hours, diluted with ether and ethyl acetate (300 mL) and then washed with water and brine before drying over MgSO4. The aqueous layer is back extracted with methylene chloride and combined with the previous organic fraction. Evaporation of solvents and chromatography (eluant 1% methanol in chloroform) and evaporation under high vacuum affords the required product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05308853
Quelldatensatzuspto-grants-1994_05
ORD IDord-b827a0970433490393d7126541b0b1b2
Quellennotizuspto-grants-1994_05