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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Methoxy-6-methyl-3-nitro-4-pyridinemethanol | HCID 15454110 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Methoxy-6-methyl-3-nitropyridine-4-carbaldehyde | HCID 2762980 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610692B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-ae5b1a02a1f148f8a657d64c063a76e1 |
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| Source note | uspto-grants-2003_08 |
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