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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108242Generated: October 26, 2026

Oxygen → Ketoprofen

https://huagongshe.com/reaction/2108242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
Reactantalpha-(3-(1-Phenylethenyl)phenyl)propionic acidHCID 14750257—
SolventAcetic AcidHCID 176—
SolventCobaltous 2-naphthenic acidHCID 14048876—
ProductKetoprofenHCID 3825—

Reaction Steps

To a 300 ml reaction vessel with a stirrer were fed 15 g of α-(3-(1-phenylethenyl)phenyl)propionic acid obtained in Example 2, 0.03 g of cobalt naphthenate and 100 ml of acetic acid as a solvent and 150 ml/min of pure oxygen was fed into the vessel for 16 hours at a reaction temperature of 120° C. After the reaction, the solvent was removed by reduced-pressure distillation to obtain a solid substance. The solid substance was washed five times with 500 ml of water and it was dissolved in 500 ml of ether and washed three times again with water. After that, the ether was removed by reduced-pressure distillation and the product was finally recrystallized with benzene/petroleum ether mixture to obtain 9.8 g of α-(3-benzoylphenyl)propionic acid (ketoprofen). The properties such as melting point and the spectrum of the final product were the same as those of an authentic sample.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04937375
Source datasetuspto-grants-1990_06
ORD IDord-03bbe13e7dd84d62ab1d95dddc0b61d1
Source noteuspto-grants-1990_06