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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779496Generated: November 2, 2026

4'-Hydroxyacetophenone → 29884-24-0

https://huagongshe.com/reaction/1779496

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-HydroxyacetophenoneHCID 7469—
ReactantPotassium CarbonateHCID 11430—
ReactantPropanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 11745—
ReactantHCID 19956261HCID 19956261—
CatalystPotassium IodideHCID 4875—
SolventMethyl Isobutyl KetoneHCID 7909—
Product29884-24-0HCID 12346108—

Reaction Steps

The ethyl 2-(4-acetylphenoxy)isobutyrate used as starting material was itself prepared as follows: 54.4 g of 4-hydroxyacetophenone, 375 ml of ethyl 2-bromoisobutyrate, 175 g of potassium carbonate, 1.2 liters of methyl isobutyl ketone and 3 g of potassium iodide are introduced into a three-necked flask equipped with a stirrer and a condenser. The whole is heated under reflux for 20 hours, then cooled, filtered and concentrated to dryness. The residue is chromatographed on 4 liters of Amicon silica (0.035-0.070 mm) while eluting with dichloromethane. The fractions retained are concentrated to dryness to yield 100 g of ethyl 2-(4-acetylphenoxy)isobutyrate in the form of a thick liquid (quantitative yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05627205
Source datasetuspto-grants-1997_05
ORD IDord-8774868f1fd04a6a8da22064c430c45b
Source noteuspto-grants-1997_05