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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651357Generated: November 2, 2026

Piperonylidene acetone → HCID 23051852, compound

https://huagongshe.com/reaction/1651357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperonylidene acetoneHCID 6040503—
ReactantGlyoxylic acid, monohydrateHCID 15620607—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 23051852HCID 23051852—

Reaction Steps

A solution of 15 g (78.8 mmol) of (E)-4-[3,4-(methylenedioxy)phenyl]but-3-en-2-one and 7.2 g (78.8 mmol) of glyoxylic acid monohydrate in 20 ml of acetic acid was heated at reflux for 20 hours. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic phase was extracted twice with 3N sodium hydroxide solution. The combined aqueous phases were treated with 3N hydrochloric acid to produce a strongly acidic reaction and extracted twice with ethyl acetate. The combined organic phases were dried over magnesium sulphate and concentrated. Crystallization of the residue from ethyl acetate/ether yielded (E,E)-6-[3,4-(methylenedioxy)phenyl]-4-oxo-2,5-hexadienoic acid of melting point 170°-173°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04927958
Source datasetuspto-grants-1990_05
ORD IDord-cd870529b9d54c86a3c4e11a54da9a60
Source noteuspto-grants-1990_05