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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 479778Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/479778

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktPhosphonic acid, P-(chloromethyl)-, diethyl esterHCID 76633—
Edukt2-Hydroxymethyl-1-methyl-4-phenyl-5-(4-pyridyl)imidazoleHCID 18771529—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelHexamethylphosphoramideHCID 12679—
ProduktDiethyl [1-methyl-4-phenyl-5-(4-pyridyl)imidazol-2-yl]methoxylmethylphosphonateHCID 86587538—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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 (mnz): 416 (M++H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06645989B2
Quelldatensatzuspto-grants-2003_11
ORD IDord-6407d6b6c7664229be44fea43f14feee
Quellennotizuspto-grants-2003_11