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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638294Generated: October 31, 2026

Sodium hydride → 2-[2-(4-Phenoxyphenoxy)ethoxy]pyridine

https://huagongshe.com/reaction/1638294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-(2-Bromoethoxy)-4-phenoxybenzeneHCID 13254487—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178516071HCID 178516071—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[2-(4-Phenoxyphenoxy)ethoxy]pyridineHCID 994850528.6%

Reaction Steps

To a suspension of sodium hydride (132 mg, 3.3 mmol; 60% in oil) in dimethylformamide (5 ml), a solution of 2-hydroxypyridine (314 mg, 3.3 mmol) in dimethylformamide (3 ml) was dropwise added with stirring, and stirring was continued at room temperature until the generation of hydrogen gas ceased. To the resultant solution, there was dropwise added a solution of 2-(4-phenoxyphenoxy)ethyl bromide (879 mg, 3.0 mmol) in dimethylformamide (3 ml), and the mixture was stirred at room temperature overnight. The reaction mixture was poured into water (70 ml) and extracted with toluene (25 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-[2-(4-phenoxyphenoxy)ethoxy]pyridine (264 mg) as white crystals. M.P., 94.2° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04879292
Source datasetuspto-grants-1989_11
ORD IDord-b5c45bf703f846dea1e854738f104c6e
Source noteuspto-grants-1989_11