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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215829Generated: October 25, 2026

Hydrochloric Acid → 3-(6-Methoxy-pyridin-3-yloxy)-benzoic acid ethyl ester

https://huagongshe.com/reaction/215829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-hydroxybenzoateHCID 24522—
Reactant5-Bromo-2-methoxypyridineHCID 2734895—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventPyridineHCID 1049—
Product3-(6-Methoxy-pyridin-3-yloxy)-benzoic acid ethyl esterHCID 6729714423.6%

Reaction Steps

A suspension of 5-bromo-2-methoxy-pyridine (5.4 g, 29 mmol), ethyl 3-hydroxybenzoate (4.0 g, 24 mmol), K2CO3 (4.3 g, 30 mmol), Cu powder (0.30 g, 4.8 mmol) and CuI (0.30 g, 1.56 mmol) in pyridine (25 ml) was refluxed for 18 h. The resulting mixture was mixed with 100 g of crushed ice, neutralized with 1N hydrochloric acid to pH 7.5 and extracted with ether. The extract was evaporated in vacuo, the obtained crude product was purified by column chromatography on silica (eluent hexanes-ethyl acetate 8:1) to afford 1.55 g (20%) of 3-(6-methoxy-pyridin-3-yloxy)-benzoic acid ethyl ester as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193192B2
Source datasetuspto-grants-2012_06
ORD IDord-44adbd6a96364be3b0f83d8ea7a0810e
Source noteuspto-grants-2012_06