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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487612Generated: October 30, 2026

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

https://huagongshe.com/reaction/487612

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 ##STR11## (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 numberUS05296490
Source datasetuspto-grants-1994_03
ORD IDord-c2581e1491514848a5ceb77809919472
Source noteuspto-grants-1994_03