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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592398Generated: October 26, 2026

Selenium Dioxide → Acetic acid 1-(2-formyl-pyridin-3-yl)-1-methyl-ethyl ester

https://huagongshe.com/reaction/1592398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSelenium DioxideHCID 24007—
ReactantAcetic acid 1-methyl-1-(2-methyl-pyridin-3-yl)-ethyl esterHCID 67272080—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductAcetic acid 1-(2-formyl-pyridin-3-yl)-1-methyl-ethyl esterHCID 8659475546.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

Selenium dioxide (1.44 g, 13.0 mmol) was added to a solution of acetic acid 1-methyl-1-(2-methyl-pyridin-3-yl)-ethyl ester (1.25 g, 6.48 mmol) dissolved in a mixture of water (2.5 mL) and 1,4-dioxane (25 mL). The resulting mixture was stirred at 100° C. for 60 hours. The solvent was removed under reduced pressure and the brown oil was quenched with saturated NaHCO3 (30 mL) and extracted with CH2Cl2 (5×50 mL). The combined organic extracts were dried (Na2SO4), filtered, and concentrated in vacuo to afford a brown oil. Purification via column chromatography on silica gel (hexanes:EtOAc, 1:1, v/v) afforded acetic acid 1-(2-formyl-pyridin-3-yl)-1-methyl-ethyl ester as a yellow oil (0.62 g, 46%). 1H NMR (CDCl3) δ 1.91 (s, 6H), 2.03 (s, 3H), 7.48 (dd, 1H, J=9.0, 6.0 Hz), 7.83 (dd, 1H, J=9.0, 3.0 Hz), 8.69 (dd, 1H, J=6.0, 3.0 Hz), 10.49 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291631B2
Source datasetuspto-grants-2007_11
ORD IDord-b62595cf7c8f499ba060dbef75af1725
Source noteuspto-grants-2007_11