HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884564Generated: October 31, 2026
Triphenylphosphine → HCID 23506266, compound
https://huagongshe.com/reaction/1884564
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Pyridinepropanol | HCID 17861 | — |
| Reactant | 2-Bromo-3-pyridinol | HCID 23070 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23506266 | HCID 23506266 | 90.5% |
Reaction Steps
3-(Pyridin-3-yl)-1-propanol (12.3 g, 90 mmol) and triphenylphosphine (34.0 g, 130 mmol) are dissolved in THF (200 ml), and thereto are added successively with stirring diisopropyl azodicarboxylate (22.2 g, 110 mmol) and 2-bromo-3-hydroxypyridine (12.0 g, 69 mmol) under ice-cooling. The mixture is stirred at room temperature for 30 minutes, and then the reaction solution is concentrated under reduced pressure. To the residue is added ethyl acetate (300 ml), and the mixture is extracted with a 10% aqueous hydrochloric acid solution (150 ml×2). The pH value of the aqueous layer is adjusted with potassium carbonate to pH 12, and the mixture is extracted with ethyl acetate (200 ml×2). The organic layer is washed with a saturated brine (50 ml×2), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography (eluent: ethyl acetate/hexane) to give the title compound (18.3 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06765095B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-366bd740838645249872467d2cd07566 |
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| Source note | uspto-grants-2004_07 |
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