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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 358285Erstellt: 23. Oktober 2026

Potassium Hydroxide → Fenoprofen

https://huagongshe.com/de/reaction/358285

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
Edukt2-Hydroxy-3-phenoxy-hydratropic acid sulphate dipotassium saltHCID 70514935—
KatalysatorNickelHCID 935—
LösungsmittelWaterHCID 962—
ProduktFenoprofenHCID 334297%

Reaktionsbedingungen

Temperatur60 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04465855
Quelldatensatzuspto-grants-1984_08
ORD IDord-42ffd2605ef546f4b2cf9b328b128d26
Quellennotizuspto-grants-1984_08