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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 358284Erstellt: 24. Oktober 2026

2-Toluene-sulphonyloxy-3-phenoxy-hydratropic acid → Fenoprofen

https://huagongshe.com/de/reaction/358284

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Toluene-sulphonyloxy-3-phenoxy-hydratropic acidHCID 20449833—
EduktHCID 178418361HCID 178418361—
KatalysatorNickelHCID 935—
ProduktFenoprofenHCID 334289%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04465855
Quelldatensatzuspto-grants-1984_08
ORD IDord-f3f0daef5bb3420fb5df1f9d4d60a4da
Quellennotizuspto-grants-1984_08