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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186877Generated: October 26, 2026

Acetic Acid → 4-(4-Hydroxyphenyl)-3-methyl-4-oxo-butyric acid ethyl ester

https://huagongshe.com/reaction/1186877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen BromideHCID 260—
Reactant4-(4-Methoxy-phenyl)-3-methyl-4-oxo-butyric acid ethyl esterHCID 14866576—
SolventEthanolHCID 702—
Product4-(4-Hydroxyphenyl)-3-methyl-4-oxo-butyric acid ethyl esterHCID 5965195245.7%

Reaction Steps

A mixture of crude 4-(4-methoxy-phenyl)-3-methyl-4-oxo-butyric acid ethyl ester (44 g, 175.8 mmol), acetic acid (300 mL) and 48% aqueous HBr (150 mL) was stirred at reflux for 10 h. The reaction was cooled to rt, concentrated at reduced pressure then partitioned between methylene chloride and water and the aqueous layer was extracted three times with methylene chloride and concentrated to provide a crude material. The crude material was dissolved in ethanol (125 mL) and added amberlyst then heated at 85° C. for 15 h. The reaction mixture was filtered over celite at rt and the filtrate was concentrated at reduced pressure and then partitioned between water and methylene chloride. The aqueous layer was extracted twice with methylene chloride to furnish a crude product and the crude product was purified by ISCO (330 g silica gel column) chromatography using 20 to 30% EtOAc in hexane to obtain a mixture (19 g) of 4-(4-hydroxyphenyl)-3-methyl-4-oxo-butyric acid ethyl ester (MS m/z 235 (M−H) and p-hydroxypropiophenone. The mixture was used for the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673916B2
Source datasetuspto-grants-2014_03
ORD IDord-097267b596e542069d7fefd5f8aecc0e
Source noteuspto-grants-2014_03