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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207667Generated: November 1, 2026

Dimethyl Sulfoxide → 4-(5-Ethoxy-2-fluoro-phenyl)-3,6-dimethyl-pyridine-2-carbaldehyde

https://huagongshe.com/reaction/2207667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant[4-(5-Ethoxy-2-fluoro-phenyl)-3,6-dimethyl-2-pyridyl]methanolHCID 89648949—
SolventDichloromethaneHCID 6344—
Product4-(5-Ethoxy-2-fluoro-phenyl)-3,6-dimethyl-pyridine-2-carbaldehydeHCID 8964907967.2%

Reaction Steps

To a solution of oxalyl chloride (1.46 mL, 17.3 mmol) in DCM (50 mL) cooled to −78° C. was added dropwise, a solution of dimethyl sulfoxide (2.68 mL, 37.74 mmol) in DCM (5 mL). After addition, the solution was stirred for 15 mins. A solution of [4-(5-ethoxy-2-fluoro-phenyl)-3,6-dimethyl-2-pyridyl]methanol (which may be prepared as described in Description 140) (4.33 g, 15.73 mmol) in DCM (10 mL) was then added dropwise over about 5 mins. The mixture was allowed to stir at −78° C. for 2 hrs. Triethylamine (8.74 mL, 62.91 mmol) was added dropwise giving a precipitate and this was allowed to warm to room temperature over one hour. The reaction mixture was washed with water and brine, dried over magnesium sulphate and evaporated. The crude residue was purified by silica gel chromatography (50 g SiO2) eluting with ethyl acetate in iso-hexane (0-40%). Evaporation of desired fractions gave 4-(5-ethoxy-2-fluoro-phenyl)-3,6-dimethyl-pyridine-2-carbaldehyde (D141) (2.89 g, 10.574 mmol, 67.2% yield) as a yellow solid;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376436B2
Source datasetuspto-grants-2016_06
ORD IDord-e3b1bf61706541189faab1076ff84df0
Source noteuspto-grants-2016_06