Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 620971Erstellt: 24. Oktober 2026

Sulfuric Acid → Ketoprofen

https://huagongshe.com/de/reaction/620971

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktSodium SulfiteHCID 24437—
EduktPotassium PermanganateHCID 516875—
Eduktalpha-(3-(1-Phenylethenyl)phenyl)propionic acidHCID 14750257—
LösungsmittelBenzeneHCID 241—
LösungsmittelWaterHCID 962—
ProduktKetoprofenHCID 3825—

Reaktionsschritte

α-(3-(1-Phenylethenyl)phenyl)propionic acid (35 g) obtained in Example 5 was dissolved in 250 ml of benzene and 250 ml of water was further added thereto with vigorous stirring to prepare a suspension. Then, 2 liter of 2% aqueous solution of potassium permanganate was dropped little by little over 1.5 hours. After the dropping, stirring was continued for 18 hours at room temperature. After the reaction, it was acidified by adding concentrated sulfuric acid and was treated by adding 35 g of sodium sulfite. After that, 500 ml of water was added and extraction was carried out three times with 150 ml of ether. The ether solution was washed with water and it was extracted three times with 200 ml of 5% aqueous solution of sodium hydroxide. It was then acidified by adding hydrochloric acid and extracted again three times with 150 ml of ether, which was followed by washing with water, drying with anhydrous magnesium sulfate, and filtration. The ether was then removed by reduced-pressure evaporation. Finally, 20 g of α-(3-benzoylphenyl)propionic acid (ketoprofen) was obtained by re-crystallization from benzene/petroleum ether mixture. The melting point and spectrum were the same as those of an authentic sample.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04822934
Quelldatensatzuspto-grants-1989_04
ORD IDord-2d92beb792e744ee80ffd7f5de272afc
Quellennotizuspto-grants-1989_04