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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840796Generated: October 30, 2026

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

https://huagongshe.com/reaction/840796

Reaction equation

Participants

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

Reaction Steps

This ester-linked benzophenone was prepared according to the method of PCT Patent Appln. No. WO 93/16131 (Everaerts et al.). In a first step, an ethyl-(4-benzoyl-phenoxy)acetate (EPBA) precursor was prepared by refluxing a mixture of 100.0 grams (0.51 moles) 4-hydroxybenizoplhenonie, 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). 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 NoM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369123B1
Source datasetuspto-grants-2002_04
ORD IDord-45601e9111fe4cbab0e320bd2a7e7661
Source noteuspto-grants-2002_04