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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648513Generated: October 29, 2026

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

https://huagongshe.com/reaction/1648513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantSodium hydrideHCID 24758—
ReactantDiethyl (2,5-dioxo-2,5-dihydro-1H-imidazol-4-yl)phosphonateHCID 53733419—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductDiethyl 1-(methoxymethyl)-2,5-dioxo-4-imidazolylphosphonateHCID 53791991—

Reaction Steps

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. MS (EI) 280

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436260
Source datasetuspto-grants-1995_07
ORD IDord-89a80d5b31b54b32b10691d2a7103986
Source noteuspto-grants-1995_07