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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073514Generated: November 2, 2026

2-Fluoropyridine → 2-{1-Methyl-2-[4-(3,5-difluorophenoxy)phenoxy]ethoxy}pyridine

https://huagongshe.com/reaction/1073514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoropyridineHCID 9746—
ReactantSodium hydrideHCID 24758—
Reactant1-Methyl-2-[4-(3,5-difluorophenoxy)phenoxy]ethanolHCID 13455913—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-{1-Methyl-2-[4-(3,5-difluorophenoxy)phenoxy]ethoxy}pyridineHCID 1338674172.2%

Reaction Steps

To a suspension of sodium hydride (20 mg, 0.5 mmol; 60% in oil) in dimethylformamide (1 ml), a solution of 1-methyl-2-[4-(3,5-difluorophenoxy)phenoxy]ethanol (140 mg, 0.5 mmol) in dimethylformamide (1 ml) was dropwise added with stirring, and stirring was continued at room temperature until the generation of hydrogen gas ceased. 2-Fluoropyridine (97 mg, 1.0 mmol) was dropwise added thereto, and the mixture was stirred at room temperature overnight. The reaction mixture was poured into water (40 ml) and extracted with toluene (20 ml) three times. The toluene layer was dried over anhydrous magnesium sulfate, and the solvent was removed by evaporation. The residue was purified by silica gel column chromatography to give 2-{1-methyl-2-[4-(3,5-difluorophenoxy)phenoxy]ethoxy}pyridine (129 mg) as pale yellow liquid. nD19.0 1.5602.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04970222
Source datasetuspto-grants-1990_11
ORD IDord-f2be74fed7cf411bb7996e7cf4c9f291
Source noteuspto-grants-1990_11