HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Toluene-sulphonyloxy-3-phenoxy-hydratropic acid → Fenoprofen
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Toluene-sulphonyloxy-3-phenoxy-hydratropic acid | HCID 20449833 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Katalysator | Nickel | HCID 935 | — |
| Produkt | Fenoprofen | HCID 3342 | 89% |
Reaktionsschritte
To a solution of 4.1 g. of 2-toluene-sulphonyloxy-3-phenoxy-hydratropic acid in 150 ml. of alcohol 24 g. of a W-6 nickel catalyst are added, and the mixture is hydrogenated at 25° C., under atmospheric pressure until a calculated amount of hydrogen is used up. The catalyst is filtered off, the filtrate is evaporated and the residue is taken up in water and acidified with a 10% aqueous hydrochloric acid solution. The separated oil is extracted with chloroform, the chloroform solution is dried over sodium sulphate and evaporated. 2.1 g. (89%) of 3-phenoxy-hydratropic acid are obtained. Melting point of the corresponding cyclohexylamine salt amounts to 151° C. to 153° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04465855 |
| Quelldatensatz | uspto-grants-1984_08 |
| ORD ID | ord-f3f0daef5bb3420fb5df1f9d4d60a4da |
| Quellennotiz | uspto-grants-1984_08 |