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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029404Generated: October 30, 2026

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

https://huagongshe.com/reaction/1029404

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 numberUS05102878
Source datasetuspto-grants-1992_04
ORD IDord-e68f4b6c308d4719a31241ae3bb01729
Source noteuspto-grants-1992_04