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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650749Generated: October 30, 2026

1-(Triphenylphosphoranylidene)acetone → 4-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-3-buten-2-one

https://huagongshe.com/reaction/1650749

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Triphenylphosphoranylidene)acetoneHCID 15038—
Reactant2-Phenylpyrazolo[1,5-a]pyridine-3-carbaldehydeHCID 15158179—
SolventBenzeneHCID 241—
Product4-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-3-buten-2-oneHCID 53900639—

Reaction Steps

A mixture of 2-phenylpyrazolo[1,5-a]-pyridine-3-carbaldehyde (0.50 g) and acetonylidenetriphenylphosphorane ##STR12## (0 82 g) in benzene (6 ml) was refluxed for 4 hours and then the solvent was evaporated in vacuo The residue was chromatographed on silica gel (20 g) with chloroform as an eluent. The fractions containing the object compound, were combined and evaporated in vacuo. The residue was recrystallized from ethanol to give crystals of 4-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)-3-buten-2-one (trans isomer) (0.21 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925849
Source datasetuspto-grants-1990_05
ORD IDord-a4a834de57ab4e769e3b546fcb93c368
Source noteuspto-grants-1990_05