HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678582Generated: November 2, 2026
3-Hydroxybenzyl alcohol → 3-(Pyridin-2-yloxy)benzaldehyde
https://huagongshe.com/reaction/1678582
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Hydroxybenzyl alcohol | HCID 102 | — |
| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-(Pyridin-2-yloxy)benzaldehyde | HCID 2735363 | 61% |
Reaction Steps
3-Hydroxybenzyl alcohol (1.0 g, 8.2 mmol) was dissolved in pyridine (20 mL). 2-Bromopyridine (1.6 g, 9.8 mmol) and potassium carbonate (2.3 g, 16.4 mmol) were added thereto, and then the mixture was stirred at 90° C. for 10 minutes. Copper oxide(II) (1.6 g, 20.5 mmol) was further added thereto, and the reaction mixture was heated under reflux for 2 days. The reaction solution was filtered, and concentrated under reduced pressure. To the residue was added water, and the mixture was extracted with ethyl acetate. The extract was dried, and then concentrated under reduced pressure. The residue was purified with silica gel column chromatography (hexane/ethyl acetate=100:0 to 70:30) to give the title compound (1.0 mg, yield 61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008525B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-6c30dd5c1b6f42d292cc86e16b1882fc |
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| Source note | uspto-grants-2011_08 |
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