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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482444Generated: October 30, 2026

Methyl iodide → diethyl 4-(3-methyl-4(3H)-quinazolinon-2-yl)benzylphosphonate

https://huagongshe.com/reaction/482444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178476844HCID 178476844—
SolventMethanolHCID 887—
Productdiethyl 4-(3-methyl-4(3H)-quinazolinon-2-yl)benzylphosphonateHCID 10643860—

Reaction Conditions

Temperature40 °C

Reaction Steps

A 5.9 g quantity of diethyl 4-(4-hydroxyquinazolin-2-yl)benzylphosphonate, 1.8 g of potassium tert-butoxide and 2.3 g of methyl iodide were suspended in 100 ml of anhydrous methanol and stirred with heating at 40° C. for 16 hours. After completion of the reaction, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (eluent: methylene chloride: methanol=100:1) and the crude crystals thus obtained were recrystallized from methylene chloride-n-hexane to provide 3.0 g of the title compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05798344
Source datasetuspto-grants-1998_08
ORD IDord-1e960697b65048cf946b43a3a37e22a9
Source noteuspto-grants-1998_08