HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613040Generated: October 23, 2026
Dimethyl Sulfoxide → 2-Chloro-4-pyridinecarboxaldehyde
https://huagongshe.com/en/reaction/613040
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | (2-Chloropyridin-4-yl)methanol | HCID 7062237 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-4-pyridinecarboxaldehyde | HCID 2762994 | — |
Reaction Steps
To a solution of oxalyl chloride (42.2 ml) in methylene chloride (1100 ml) is added dropwise a solution of dimethyl sulfoxide (68.7 ml) in methylene chloride (220 ml) at -60° C. to -50° C., and thereto is further added dropwise a solution of 2-chloro-4-hydroxymethylpyridine (63.2 g) in methylene chloride (440 ml) at the same temperature. The mixture is stirred for 15 minutes, and thereto is added dropwise triethylamine (306.6 ml) at the same temperature. The mixture is stirred for five minutes, and warmed to room temperature. After the reaction is complete, to the reaction mixture is added water (2.2 liters). The methylene chloride layer is separated, and the aqueous layer is extracted again with methylene chloride (2.2 liters). The methylene chloride layers are combined, and washed with a saturated aqueous sodium hydrogen carbonate solution, dried, and concentrated under reduced pressure to remove the solvent to give 2-chloropyridine-4-carbaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06005106 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-989c8ee156ce4cb5948ec454ce9163f9 |
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| Source note | uspto-grants-1999_12 |
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