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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536082Generated: November 3, 2026

Water → 6-Ethoxypyridine-2-carbaldehyde

https://huagongshe.com/reaction/536082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant(6-Ethoxypyridin-2-yl)methanolHCID 53393171—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
Product6-Ethoxypyridine-2-carbaldehydeHCID 4508373070.9%

Reaction Conditions

Temperature-60 °C

Reaction Steps

DMSO (0.50 mL, 6.4 mmol) in CH2Cl2 (10 mL) was added dropwise to a solution of oxalyl chloride (2M in CH2Cl2, 3.1 mL, 6.1 mmol) in CH2Cl2 (20 mL) at −60° C. The resulting mixture was stirred at −60° C. for 10 minutes. (6-Ethoxy-pyridin-2-yl)-methanol (0.85 g, 5.6 mmol) in CH2Cl2 (5 mL) and DMSO (4 mL) was added dropwise. The mixture was stirred at −60° C. for 3 h, and was then allowed to warm to −20° C. and Et3N (6 mL) was added. The resulting solution was stirred at ambient temperature for 40 minutes. Water was added and the mixture was extracted with CH2Cl2. The organic phase was washed with brine, dried (Na2SO4), and concentrated. Diethyl ether was added to the residue and insoluble material was removed by filtration. The filtrate was concentrated to yield the title compound (0.60 g) in 70% yield as a solid. This crude product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859568B2
Source datasetuspto-grants-2014_10
ORD IDord-5f566f96b7594723a5be6016d3d721d6
Source noteuspto-grants-2014_10