HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837814Generated: October 28, 2026
Hydrogen Peroxide → 4-(Pyridin-2-yloxy)phenol
https://huagongshe.com/reaction/1837814
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Boric Acid | HCID 7628 | — |
| Reactant | 4-(Pyridin-2-yloxy)benzaldehyde | HCID 3755292 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Pyridin-2-yloxy)phenol | HCID 14652373 | 9.6% |
Reaction Steps
Following Scheme I: To a 100 mL round-bottomed flask equipped with condenser and N2 inlet were added 3.1 g (50.2 mmol) boric acid, 10 mL tetrahydrofuran, 2.3 mL (20 mmol) 30% hydrogen peroxide, and 1 mL concentrated sulfuric acid. To the reaction was added a solution of 2.0 g (10 mmol) 4-(pyridin-2-yloxy)-benzaldehyde in 10 mL tetrahydrofuran dropwise over 5 minutes. The reaction was stirred 3 hr at 60° C., cooled, filtered, and the filtrate neutralized with saturated aqueous sodium bicarbonate solution. The mixture was extracted into 2× ethyl acetate, and the organic layer washed with brine, dried over sodium sulfate, and evaporated. The residue was chromatographed on silica gel using hexane/ethyl acetate as eluant to afford 180 mg (9.6%) of the product as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06784299B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-44bb32691a94416ba1d3abe808a842d6 |
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| Source note | uspto-grants-2004_08 |
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