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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465559Generated: November 1, 2026

Cesium carbonate → 1-{4-((5-Methoxypyridin-2-yl)oxy)-2,6-dimethylphenyl}ethanone

https://huagongshe.com/reaction/1465559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantN,N-Dimethylglycine hydrochlorideHCID 75605—
Reactant1-(4-Hydroxy-2,6-dimethylphenyl)ethanoneHCID 4057370—
Reactant2-Bromo-5-methoxypyridineHCID 11148151—
CatalystCopper iodideHCID 83717—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product1-{4-((5-Methoxypyridin-2-yl)oxy)-2,6-dimethylphenyl}ethanoneHCID 86690862107%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-bromo-5-methoxypyridine (18-1, 1.03 g, 5.46 mmol), 1-(4-hydroxy-2,6-dimethylphenyl)ethanone (4-2, 0.80 g, 4.89 mmol), N,N-dimethylglycine HCl salt (0.28 g, 1.95 mmol), copper iodide (0.24 g, 1.24 mmol), and cesium carbonate (3.57 g, 10.96 mmol) in dioxane (10 mL) was heated at 120° C. for 4.0 h. The reaction mixture was cooled to room temperature, added with water, and extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous MgSO4, and concentrated to give 1-{4-((5-methoxypyridin-2-yl)oxy)-2,6-dimethylphenyl}ethanone (18-2, 1.42 g) as a yellow oil in 96% yield, which was used directly for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999983B2
Source datasetuspto-grants-2015_04
ORD IDord-213196f336134868a8f83dc613ba295c
Source noteuspto-grants-2015_04