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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076327Generated: October 31, 2026

Methyl Acrylate → 4-(m-Methylcinnamyl)-4-phenyl-5-oxo-7-(p-chlorophenyl)-6-heptenoic Acid

https://huagongshe.com/reaction/1076327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
Reactant1-(p-Chlorophenyl)-4-phenyl-7-(m-methylphenyl)-1,6-heptadien-3-oneHCID 54166609—
SolventMethanolHCID 887—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(m-Methylcinnamyl)-4-phenyl-5-oxo-7-(p-chlorophenyl)-6-heptenoic AcidHCID 54047553—

Reaction Steps

Triton B (2 ml., 40% in MeOH) is added to a stirred solution of 1-(p-chlorophenyl)-4-phenyl-7-(m-methylphenyl)-1,6-heptadien-3-one (19.33 g., 0.05 mole) in glyme (250 ml.) followed by the addition of methyl acrylate (4.73 g., 0.055 mole) in glyme (50 ml.). The solution is stirred for 96 hours and the solvent is removed under reduced pressure. The residue is suspended in methanol (700 ml.) and a 20% sodium hydroxide solution (35 ml.) is added. After an additional 24 hours, the methanol is evaporated in vacuo and the residue is dissolved in water. Extraction with ether removes unreacted ketone. The aqueous solution is acidified and the solid that separates is collected, washed well with water, and air-dried, yield 9.78 g., m.p. 135°-144°C. Recyrstallization from butyl chloride produces material with m.p. 154°-155°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03956374
Source datasetuspto-grants-1976_05
ORD IDord-29090e2d2fda4bf58e119ef5fd19eff9
Source noteuspto-grants-1976_05