HuagongsheHuagongshe Chemistry Print Report · For research reference only
Selenium Dioxide → 6-(2-Bromophenyl)picolinaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | 6-(2-Bromophenyl)-2-methylpyridine | HCID 20184690 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-(2-Bromophenyl)picolinaldehyde | HCID 20184679 | 54.1% |
Reaction Steps
6-(2-bromophenyl)-2-methylpyridine (3.5 g) was dissolved in 150 ml 1,4-dioxane. Selenium dioxide (Aldrich, Gold Label, 2.0 g) was added and the mixture was refluxed for a total of 50 hours. The solids were removed by filtration and the mixture was diluted with ether. The solution was washed several times with water, dried over magnesium sulfate, filtered and evaporated to afford 2.0 g of crude 6-(2-bromophenyl)-2-pyridinecarboxaldehyde as a yellow semi-solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04696938 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-75e7260bb95d44a1aa0c2334fa9a0529 |
| Source note | uspto-grants-1987_09 |