HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578593Generated: October 30, 2026
Selenium Dioxide → 4-(3-Chloropyridin-2-yl)benzaldehyde
https://huagongshe.com/reaction/578593
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | 3-Chloro-2-(p-tolyl)pyridine | HCID 20709936 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(3-Chloropyridin-2-yl)benzaldehyde | HCID 53426238 | 85% |
Reaction Steps
100 g (0.49 mol) of 3-chloro-2-para-tolylpyridine was dissolved in 1 L of 1,4-dioxane in a reactor. 163.4 g (1.47 mol) of selenium dioxide was added, and the mixture was refluxed for 4˜6 hours. The reaction solution was cooled to 25° C., and floating matter was filtered off with celite. A 10% sodium bicarbonate solution was added, and the mixture was extracted with ethyl acetate. The organic layer was dried with magnesium sulfate and concentrated under reduced pressure, yielding 4-(3-chloropyridin-2-yl)benzaldehyde as represented below in a 85% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040572B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-9d72973adc8b4788893c4d0b0397c29a |
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| Source note | uspto-grants-2015_05 |
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