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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293512Generated: October 26, 2026

Sodium hydride → Diethyl [1-methyl-4-phenyl-5-(4-pyridyl)imidazol-2-yl]methoxylmethylphosphonate

https://huagongshe.com/reaction/2293512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantPhosphonic acid, P-(chloromethyl)-, diethyl esterHCID 76633—
Reactant2-Hydroxymethyl-1-methyl-4-phenyl-5-(4-pyridyl)imidazoleHCID 18771529—
SolventDimethylformamideHCID 6228—
SolventHexamethylphosphoramideHCID 12679—
ProductDiethyl [1-methyl-4-phenyl-5-(4-pyridyl)imidazol-2-yl]methoxylmethylphosphonateHCID 86587538—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 80% NaH in mineral oil (0.013 g, 0.452 mmol) in DMF at 0° C. was added 1-methyl-2-hydroxymethyl-4-phenyl-5-[4-pyridinyl]imidazole (0.100 g, 0.377 mmol) in DMF. The resulting bright yellow solution was stirred at 0° C. for 0.5 h when diethyl chloromethylphosphonate (0.070 mL, 0.452 mmol) dissolved in 0.079 mL, of HMPA was added. The resulting mixture was stirred at 0° C. for 15 min and then warmed to rt. After 5 h, the solution was partitioned between CH2Cl2 and H2O. The organic extract was washed with aqueous NaCl and dried (MgSO4). The solvent was removed in vacuo, and the residue was purified by flash chromatography, eluting with 50:1 CH2Cl2 /MeOH. The title compound was obtained as a light amber oil (0.088 g, 56%): ESMS (m/z): 416 (M+ +H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05686455
Source datasetuspto-grants-1997_11
ORD IDord-67d228a4796745c888f35b5bbe6d1764
Source noteuspto-grants-1997_11