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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSelenium DioxideHCID 24007—
Reactant3-(2-Ethoxyethoxy)-2-methylpyridineHCID 67068475—
Solvent1,4-DioxaneHCID 31275—
Product3-(2-Ethoxyethoxy)pyridine-2-carbaldehydeHCID 8662312939%

Reaction Conditions

Temperature75 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859568B2
Source datasetuspto-grants-2014_10
ORD IDord-1353b5d05d954d19a31d3fe773a67420
Source noteuspto-grants-2014_10