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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075498Generated: October 30, 2026

Potassium Iodide → 1-(6-Chloro-pyridin-3-ylmethoxy)-naphthalene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/2075498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2,4,6-Tris((dimethylamino)methyl)phenolHCID 7026—
ReactantCesium carbonateHCID 10796—
Reactant2-Naphthalenecarboxylic acid, 1-hydroxy-, methyl esterHCID 70358—
Reactant2-Chloro-5-(chloromethyl)pyridineHCID 155479—
SolventWaterHCID 962—
Product1-(6-Chloro-pyridin-3-ylmethoxy)-naphthalene-2-carboxylic acid methyl esterHCID 8661967499.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 1.0 g 1-hydroxy-2-naphthoic acid methyl ester in 20 ml abs. DMF 3.22 g cesium carbonate was added, followed by addition of 0.16 g potassium iodide and 0.96 g 2-chloro-5-chloromethyl-pyridine. Under argon-atmosphere the reaction mixture was heated to 60° C. for 1 h. The mixture was then poured into water and extracted with ethyl acetate at pH9 three times. The combined organic layers were dried over magnesium sulphate, filtrated and after removal of the solvent a crude product was obtained which was recrystallized from diethyl ether to yield 1.62 g 1-(6-chloro-pyridin-3-ylmethoxy)-naphthalene-2-carboxylic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919628B2
Source datasetuspto-grants-2011_04
ORD IDord-22116be38d2e46a28dfd57073a36f7df
Source noteuspto-grants-2011_04