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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(2-Bromoethoxy)-4-phenoxybenzene | HCID 13254487 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178516071 | HCID 178516071 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[2-(4-Phenoxyphenoxy)ethoxy]pyridine | HCID 9948505 | 28.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04879292 |
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| Source dataset | uspto-grants-1989_11 |
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| ORD ID | ord-b5c45bf703f846dea1e854738f104c6e |
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| Source note | uspto-grants-1989_11 |
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