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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 478092생성일: 2026년 10월 25일

Water → Ketoprofen

https://huagongshe.com/reaction/478092

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sulfuric AcidHCID 1118—
반응물Sodium SulfiteHCID 24437—
반응물Potassium PermanganateHCID 516875—
반응물HCID 14423576HCID 14423576—
용매BenzeneHCID 241—
생성물KetoprofenHCID 3825—

반응 단계

α-(3-(1-Phenylethenyl)phenyl)propionaldehyde (36 g) obtained in Example 4 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 with 5% aqueous solution of sodium hydroxide. The aqueous layer was acidified by adding hydrochloric acid and extracted again with 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04889952
출처 데이터셋uspto-grants-1989_12
ORD IDord-dfb0c96781cd4563a5f91b0a45e8d931
출처 메모uspto-grants-1989_12