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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974021Generated: October 24, 2026

Malonic Acid → 3-(4-Phenylphenyl)prop-2-enoic acid

https://huagongshe.com/en/reaction/974021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMalonic AcidHCID 867—
ReactantPiperidineHCID 8082—
Reactant(1,1'-Biphenyl)-4-carboxaldehydeHCID 76689—
SolventPyridineHCID 1049—
Product3-(4-Phenylphenyl)prop-2-enoic acidHCID 2549276.2%

Reaction Steps

A mixture of 4-phenylbenzaldehyde (5.17 g, 28.4 mmol), malonic acid (4.0 g), pyridine (20 ml), and piperidine (0.5 ml) was heated until gas evolution began. Heating was continued until gas evolution ceased (about 30 minutes at 90°-100° C.). The mixture was cooled, and the solid product triturated with boiling methanol (150 ml) and enough concentrated HCl to make the mixture acidic. The mixture was cooled, and the product collected by filtration, washed with water and methanol, and dried in vacuo to provide 4-phenylcinnamic acid (4.85 g, 76% yield), mp 220°-225° C. This material was dissolved in ethanol (150 ml) containing concentrated sulfuric acid (0.5 ml) and triethyl orthoacetate (3.5 ml), and refluxed for 24 hours. Removal of the solvent and recrystallization of the residue from methanol-water provided the ethyl ester (5.0 g, 92% yield), mp 88°-89° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05066658
Source datasetuspto-grants-1991_11
ORD IDord-e3f377d3f72849ed9be058409a8f0fd8
Source noteuspto-grants-1991_11