Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | alpha-(3-(1-Phenylethenyl)phenyl)propionic acid | HCID 14750257 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Cobaltous 2-naphthenic acid | HCID 14048876 | — |
| Product | Ketoprofen | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04937375 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-03bbe13e7dd84d62ab1d95dddc0b61d1 |
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| Source note | uspto-grants-1990_06 |
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