HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536091Generated: October 30, 2026
Ethyl Acetate → 3-(2-Ethoxyethoxy)pyridine-2-carbaldehyde
https://huagongshe.com/reaction/536091
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | 3-(2-Ethoxyethoxy)-2-methylpyridine | HCID 67068475 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(2-Ethoxyethoxy)pyridine-2-carbaldehyde | HCID 86623129 | 39% |
Reaction Steps
A mixture of 3-(2-ethoxyethoxy)-2-methylpyridine (0.506 g, 2.79 mmol) and selenium dioxide (0.31 g, 2.79 mmol) in 1,4-dioxane (10 mL) was heated at 75° C. overnight. After cooling to r.t., the mixture was filtered and the solids were washed with ethyl acetate. The solvent was removed in vacuo. The reaction was not complete and the solid was dissolved in 1,4 dioxane (15 mL) and selenium dioxide (0.31 g, 2.79 mmol) was added. The mixture was heated at 110° C. overnight. Ethyl acetate (10 mL) was added and the mixture was filtered. The black solid was washed with ethyl acetate and the filtrate was evaporated in vacuo. The crude product was purified by flash column chromatography (heptane/ethyl acetate gradient; 0 to 100% ethyl acetate), obtaining 0.21 g (39%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859568B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-1353b5d05d954d19a31d3fe773a67420 |
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| Source note | uspto-grants-2014_10 |
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