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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706268Generated: November 1, 2026

4-Pyridinecarboxaldehyde → HCID 53658794, compound

https://huagongshe.com/reaction/1706268

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridinecarboxaldehydeHCID 13389—
ReactantSodium hydrideHCID 24758—
ReactantHCID 20337426HCID 20337426—
SolventDimethyl SulfoxideHCID 679—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53658794HCID 53658794—

Reaction Steps

A mixture of 3-(2,5-dimethoxyphenyl)butyl triphenylphosphonium bromide (19.0 g., 35.4 mmoles) in dimethylsulfoxide (50 ml.) is added to 4-pyridinecarboxaldehyde (3.79 g., 35.4 mmoles) in tetrahydrofuran (40 ml.). The resulting mixture is then added dropwise to a slurry of 50% sodium hydride (1.87 g., 39 mmoles) in tetrahydrofuran (20 ml.) under a nitrogen atmosphere at 0°-5° C. Following completion of addition, the mixture is stirred for one hour at 0°-5° and then concentrated under reduced pressure. The concentrate is diluted with water (200 ml.) and then acidified with 6 N HCl. The aqueous acid solution is extracted with benzene (4×50 ml.). It is then made basic and extracted with ethyl acetate (3×50 ml.). Evaporation of the combined extracts after drying (MgSO4) affords 4-(2,5-dimethoxyphenyl)-1-(4-pyridyl)-1-pentene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04206225
Source datasetuspto-grants-1980_06
ORD IDord-6f4634794f624127b02b476ef932e696
Source noteuspto-grants-1980_06