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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326175Generated: October 30, 2026

4-Hydroxybenzaldehyde → HCID 682482, compound

https://huagongshe.com/reaction/326175

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
Reactant4-MethylpyridineHCID 7963—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 682482HCID 68248282.7%

Reaction Steps

In 65.8 g of acetic anhydride, 20.0 g of γ-picolin and 26.2 g of p-hydroxybenzaldehyde were refluxed for 24 hours. The resultant reaction mixture and 100 ml of 6 N hydrochloric acid added thereto were further refluxed for 60 minutes and then cooled. The reaction product was neutralized by addition of aqueous ammonia and stirred for 1 hour. The yellow crystals which consequently deposited therein were separated by filtration. The crystals were recrystallized from a mixed solvent of ethanol and ether, to afford 35 g of 4-[2-(4-hydroxyphenyl)-ethenyl]-pyridine having a melting point of 272° to 275° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04444868
Source datasetuspto-grants-1984_04
ORD IDord-0058906b35ad4192b1bd407670a0ca5e
Source noteuspto-grants-1984_04