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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948274Generated: October 25, 2026

Sodium Iodide → 1-(4-chlorobenzyl)-5-(4-fluorophenoxy)pyridin-2(1H)-one

https://huagongshe.com/reaction/1948274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
Reactant5-(4-Fluorophenoxy)-2-methoxypyridineHCID 44254192—
SolventAcetonitrileHCID 6342—
Product1-(4-chlorobenzyl)-5-(4-fluorophenoxy)pyridin-2(1H)-oneHCID 5896692127%

Reaction Steps

According to Scheme 32 Step 1: 5-(4-Fluorophenoxy)-2-methoxypyridine (2.37 mmol, 520 mg), 4-chlorobenzylchloride (3.55 mmol, 603 mg), NaI (2.37 mmol, 356 mg) in acetonitrile (15 mL) was heated at 150° C. for 20 minutes under microwave conditions. The cooled crude reaction washed with water, extracted with AcOEt. The organic layer was collected, dried (Na2SO4) and the solvent was evaporated under reduced pressure. The residue was purified in a manifold (vac.) using a Sep-Pak silica cartridge (heptane/AcOEt, 90:10 to CH2Cl2) and then CH2Cl2/acetone 90:10), following HPLC purification yielding 1-(4-chlorobenzyl)-5-(4-fluorophenoxy)pyridin-2(1H)-one (211 mg, 27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399493B2
Source datasetuspto-grants-2013_03
ORD IDord-8be4dd2a51f44dc6a36bff4fdc097106
Source noteuspto-grants-2013_03