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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651355Generated: November 2, 2026

(3E)-4-(3-methoxyphenyl)but-3-en-2-one → HCID 23051864, compound

https://huagongshe.com/reaction/1651355

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3E)-4-(3-methoxyphenyl)but-3-en-2-oneHCID 2560578—
ReactantGlyoxylic acid, monohydrateHCID 15620607—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 23051864HCID 23051864—

Reaction Steps

A solution of 14.7 g (83.4 mmol) of (E)-4-(3-methoxyphenyl)but-3-en-2-one and 7.67 g (83.4 mmol) of glyoxylic acid monohydrate in 21.2 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 ether/ethyl acetate yielded (E,E)-6-(3-methoxyphenyl)-4-oxo-2,5-hexadienoic acid of melting point 158°-160°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04927958
Source datasetuspto-grants-1990_05
ORD IDord-3c2143c3e108462e96191b8fe7e706bb
Source noteuspto-grants-1990_05