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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988829Generated: November 5, 2026

Potassium Carbonate → 4-[(4-Fluorophenyl)methoxy]-3-nitropyridine

https://huagongshe.com/reaction/1988829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Fluorobenzylic alcoholHCID 68022—
ReactantEthanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
Reactant4-Chloro-3-nitropyridineHCID 2735781—
SolventTolueneHCID 1140—
Product4-[(4-Fluorophenyl)methoxy]-3-nitropyridineHCID 6870341686.3%

Reaction Steps

4-Chloro-3-nitropyridine (2.0 g, 12.62 mmol) prepared in Step 1 of Preparation 1 was added to a suspension of 4-fluorobenzyl alcohol (2.04 ml, 18.92 mmol), potassium carbonate (1.74 g, 12.62 mmol), and potassium hydroxide (2.38 g, 50.48 mmol) in anhydrous toluene (100 ml). A catalytic amount of tris[2-(2-methoxyethoxy)ethyl]amine was added to the reaction mixture, which was then stirred for 1 hour at room temperature. The reaction mixture was filtered and then concentrated under reduced pressure. The resulting residue was purified with silica gel column chromatography (ethyl acetate/n-hexane=1/1, (v/v)) to give the titled compound as a white solid (2.5 g, 86.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642269B2
Source datasetuspto-grants-2010_01
ORD IDord-6bb0bbb85b0946319ed56200dc5d8de6
Source noteuspto-grants-2010_01