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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207594Generated: November 2, 2026

Dimethyl Sulfoxide → 4-Bromo-3-methyl-2-pyridinecarboxaldehyde

https://huagongshe.com/reaction/2207594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant(4-Bromo-3-methylpyridin-2-YL)methanolHCID 72210858—
SolventDichloromethaneHCID 6344—
Product4-Bromo-3-methyl-2-pyridinecarboxaldehydeHCID 7220995094.1%

Reaction Steps

To a stirred and cooled (−78° C.) solution of oxalyl chloride (2.82 mL, 33.37 mmol) in DCM (70 mL) under nitrogen was added dropwise a solution of dimethyl sulfoxide (5.17 mL, 72.81 mmol) in DCM (10 mL). Stirring was continued for 10 minutes. A solution of (4-bromo-3-methyl-2-pyridyl)methanol (which may be prepared as described in Description 6) (6130 mg, 30.34 mmol) in DCM (35 mL) was then added dropwise over 20 minutes. The reaction was then allowed to stir for 1 hour. Triethylamine (18.98 mL, 136.53 mmol) was then added dropwise and the reaction was allowed to warm to room temperature over 1.5 hours. The reaction was then quenched by addition of water (approximately 100 mL). The organics were separated and washed with additional water (150 mL). The organics were dried using a hydrophobic frit and concentrated in vacuo to give 4-bromo-3-methyl-pyridine-2-carbaldehyde (D7) (5.709 g, 28.541 mmol, 94.1% yield) as a brown oil which crystallised on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376436B2
Source datasetuspto-grants-2016_06
ORD IDord-26786f995b69461596769ccc7d961c04
Source noteuspto-grants-2016_06