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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267942Generated: November 1, 2026

Triphenylphosphine → HCID 23506266, compound

https://huagongshe.com/reaction/1267942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-PyridinepropanolHCID 17861—
Reactant2-Bromo-3-pyridinolHCID 23070—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23506266HCID 2350626690.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555557B1
Source datasetuspto-grants-2003_04
ORD IDord-bcf3b4f12d1848c0a1634063bcf39321
Source noteuspto-grants-2003_04