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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579941Generated: October 30, 2026

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

https://huagongshe.com/reaction/579941

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 numberUS04751225
Source datasetuspto-grants-1988_06
ORD IDord-6846000d463643cebfa0ec92f60ea9ac
Source noteuspto-grants-1988_06