Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291348Generated: October 31, 2026

4-Hydroxybenzaldehyde → P-hydroxyl ethyl cinnaMate

https://huagongshe.com/reaction/2291348

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantPiperidineHCID 8082—
ReactantPropanedioic acid, monoethyl esterHCID 3595298—
SolventPyridineHCID 1049—
ProductP-hydroxyl ethyl cinnaMateHCID 34917280.1%

Reaction Steps

To 20 g of p-hydroxybenzaldehyde and 32.5 g of monoethyl malonate were added 6 ml of pyridine and 0.2 ml of piperidine, then the mixture thus obtained was heated at 100° to 110° C. for 10 hours under stirring. The reaction mixture was then cooled, extracted with chloroform, and the chloroform layer was washed with an aqueous solution saturated with potassium hydrogen sulfite and water in this order, the chloroform extract was dried with anhydrous magnesium sulfate. The solvent was removed by evaporation and the residue thus obtained was crystallized from isopropyl ether-n-hexane to yield 25.2 g of ethyl 4-hydroxycinnamate. Light yellow indefinite form crystals. Melting point: 70°-71° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04795814
Source datasetuspto-grants-1989_01
ORD IDord-4ac18748e86d47c188c0ae10236b2587
Source noteuspto-grants-1989_01