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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | (4-Bromo-3-methylpyridin-2-YL)methanol | HCID 72210858 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-3-methyl-2-pyridinecarboxaldehyde | HCID 72209950 | 94.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376436B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-26786f995b69461596769ccc7d961c04 |
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| Source note | uspto-grants-2016_06 |
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