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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654548Generated: October 31, 2026

Benzophenone → Acetic acid, (4-benzoylphenoxy)-, ethyl ester

https://huagongshe.com/reaction/1654548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenoneHCID 3102—
ReactantAcetophenoneHCID 7410—
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant4-HydroxybenzophenoneHCID 14347—
SolventMethyl Ethyl KetoneHCID 6569—
ProductAcetic acid, (4-benzoylphenoxy)-, ethyl esterHCID 4686517—

Reaction Steps

This molecule is an important precursor for the synthesis of the multifunctional acetophenone and benzophenone crosslinking agents disclosed in this application. The ethyl-(4-benzoyl-phenoxy)acetate was prepared by refluxing a mixture of 100.0 grams (0.51 moles) 4-hydroxybenzophenone, 85.2 grams (0.51 moles) ethyl bromoacetate and 800 ml of 2-butanone (MEK) in the presence of an excess of potassium carbonate (209 grams or 1.5 moles). After three hours, the carbonate was filtered off and the MEK removed on a rotovapor. The residue was crystallized from isopropyl alcohol to yield a white, flaky product with a sharp melting point of 82° C. The structure was confirmed by NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05407971
Source datasetuspto-grants-1995_04
ORD IDord-4fc385aace7b45d4af3f3bd4be529699
Source noteuspto-grants-1995_04