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HRID 478092作成日:2026年10月26日

Water → Ketoprofen

https://huagongshe.com/reaction/478092

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sulfuric AcidHCID 1118—
反応物Sodium SulfiteHCID 24437—
反応物Potassium PermanganateHCID 516875—
反応物alpha-(3-(1-Phenylethenyl)phenyl)propionaldehydeHCID 14423576—
溶媒BenzeneHCID 241—
生成物KetoprofenHCID 3825—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04889952
出典データセットuspto-grants-1989_12
ORD IDord-dfb0c96781cd4563a5f91b0a45e8d931
出典メモuspto-grants-1989_12