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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521758Generated: October 26, 2026

Cesium carbonate → 3-(2-Bromo-pyridin-4-yloxy)-benzoic acid

https://huagongshe.com/reaction/521758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 3-HydroxybenzoateHCID 88068—
Reactant2-Bromo-4-chloropyridineHCID 2762836—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product3-(2-Bromo-pyridin-4-yloxy)-benzoic acidHCID 58167936—

Reaction Conditions

Temperature66 °C

Reaction Steps

A mixture of 2-bromo-4-chloro-pyridine (200 mg, 1.04 mmol), methyl-3-hydroxybenzoate (158 mg, 1.04 mmol), cesium carbonate (507 mg, 1.56 mmol) in 10 ml of anhydrous DMSO was heated at 66° C. for 5 hours. The mixture was diluted with ethyl acetate (100 ml), washed with brine (3×50 ml), dried over Na2SO4 and evaporated to give a colorless oil. The oil was dissolved in MeOH (8 ml), and 2M NaOH solution (4 ml, 8 mmol) was added. The mixture was heated at 60° C. for 20 minutes, poured into 50 ml of water, and acidified to pH=4. The precipitates were filtered, washed with water and dried in vacuo to give 3-(2-bromo-pyridin-4-yloxy)-benzoic acid as white solid. Yield: 170 mg, 56%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328103B2
Source datasetuspto-grants-2016_05
ORD IDord-f29c056ee6d54b999a20a8210d7db75c
Source noteuspto-grants-2016_05