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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398334Generated: October 30, 2026

Dimethyl Sulfoxide → 2-Methoxy-6-methyl-3-nitropyridine-4-carbaldehyde

https://huagongshe.com/reaction/398334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Methoxy-6-methyl-3-nitro-4-pyridinemethanolHCID 15454110—
SolventDichloromethaneHCID 6344—
Product2-Methoxy-6-methyl-3-nitropyridine-4-carbaldehydeHCID 2762980—

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a −70° C. solution of oxalyl chloride (2.0 mL, 22 mmol) in 50 mL of DCM was added 3.4 mL (44 mmol) of DMSO in 10 mL of DCM by dropping funnel. After 2 min, the reaction mixture was treated with 3.99 g (20 mmol) of the alcohol from step C in 20 mL of DCM. The solution was stirred for an additional 15 min at −70° C., treated with 14 mL (50 mmol) of Et3N and warmed to ambient temperature over 90 min. The reaction was quenched with 100 mL of water and the two phases were separated. The aqueous phase was extracted with 100 mL of DCM and the combined organic extracts were washed with 50 mL of brine and dried over MgSO4. The yellow solution was concentrated and chromatographed (2:3 EtOAc/Hexane) to afford the aldehyde as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610692B1
Source datasetuspto-grants-2003_08
ORD IDord-ae5b1a02a1f148f8a657d64c063a76e1
Source noteuspto-grants-2003_08