Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 2-Hydroxy-3-phenoxy-hydratropic acid sulphate dipotassium salt | HCID 70514935 | — |
| Katalysator | Nickel | HCID 935 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Fenoprofen | HCID 3342 | 97% |
Reaktionsschritte
To a solution of 4.2 g. of 2-hydroxy-3-phenoxy-hydratropic acid sulphate dipotassium salt in 50 ml. of water 2 g. of potassium hydroxide and 2 g. of a Raney nickel catalyst prepared freshly according to Urashibara, and the reaction mixture is stirred at 60° C. for 10 to 15 minutes. The catalyst is filtered off and the filtrate is acidified with a 20% aqueous hydrochloric acid solution. The separated solution is extracted with chloroform and the chloroform solution is dried over sodium sulphate and evaporated. 2.35 g. (97%) of 3-phenoxy-hydratropic acid are obtained. Melting point of the corresponding cyclohexylamine salt: 151° C. to 153° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04465855 |
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| Quelldatensatz | uspto-grants-1984_08 |
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| ORD ID | ord-42ffd2605ef546f4b2cf9b328b128d26 |
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| Quellennotiz | uspto-grants-1984_08 |
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