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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207603Generated: November 2, 2026

Dimethyl Sulfoxide → 4-Bromo-5-methylpicolinaldehyde

https://huagongshe.com/reaction/2207603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant(4-Bromo-5-methylpyridin-2-yl)methanolHCID 23114663—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-Bromo-5-methylpicolinaldehydeHCID 7172097461.8%

Reaction Steps

A solution of dimethyl sulfoxide (0.85 mL, 12.02 mmol) in DCM (10 mL) was added dropwise over 5 minutes to a solution of oxalyl chloride (0.47 mL, 5.51 mmol) in DCM (20 mL) at −78° C. under an atmosphere of N2 (gas evolved). Stirring was continued for 10 minutes. To this solution was added (4-bromo-5-methyl-2-pyridyl)methanol [CAS: 820224-83-7](1.01 g, 5.01 mmol) in DCM (2 mL) dropwise over a period of 10 minutes. Stirring was then continued for a further 10 minutes. Triethylamine (3.13 mL, 22.54 mmol) was added dropwise and stirring continued for 5 minutes, before allowing the reaction to warm to room temperature. Water was added and the phases were separated by passing over a hydrophobic frit. The organic phase was evaporated to yield a dark brown solid which was dried under vacuum overnight (795 mg). This was purified by column chromatography on silica gel (0-100% EtOAc in isohexane) to yield 4-bromo-5-methyl-pyridine-2-carbaldehyde (D21) (619 mg, 3.0945 mmol, 61.8% yield) as an orange crystalline solid;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376436B2
Source datasetuspto-grants-2016_06
ORD IDord-2793f04076724782abdedcd1cf56a4ac
Source noteuspto-grants-2016_06