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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650017Generated: November 2, 2026

Benzophenone → 3-Ethylbenzophenone

https://huagongshe.com/reaction/1650017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenoneHCID 3102—
ReactantDiethyl SulfateHCID 6163—
ReactantAluminum(III) ChlorideHCID 6451240—
Product3-EthylbenzophenoneHCID 583730—

Reaction Steps

Friedel-Crafts alkylation is carried out with benzophenone and diethyl sulfate in the presence of aluminum chloride to form 3-ethylbenzophenone. It is then subjected to bromination using N-bromosuccinimide to produce 3-(1-bromoethyl)benzophenone, which is then subjected to alkali hydrolysis to obtain 3-(1-hydroxyethyl)benzophenone. This compound is further reacted with carbon monoxide to obtain ketoprofen (Spanish Patent No. 452,500). ##STR4##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04922052
Source datasetuspto-grants-1990_05
ORD IDord-8ca69273dd56416994935a28a98e1360
Source noteuspto-grants-1990_05