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

HRID 358284

Reaktionsgleichung

Reaktionsgleichung von HRID 358284
C1(C)C(S(O[C:11]2[C:21]([O:22][C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)=[CH:20][CH:19]=[CH:18][C:12]=2[CH:13]([CH3:17])[C:14]([OH:16])=[O:15])(=O)=O)=CC=CC=1.[H][H]>[Ni]>[O:22]([C:21]1[CH:11]=[C:12]([CH:18]=[CH:19][CH:20]=1)[CH:13]([CH3:17])[C:14]([OH:16])=[O:15])[C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1

Komponenten

4

Edukt 2

HCID 204498332-Toluene-sulphonyloxy-3-phenoxy-hydratropic acidHCID 178418361HCID 178418361, Verbindung

Produkt 1

HCID 3342FenoprofenAusbeute 89 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 935NickelKatalysator

Versuchsvorschrift

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.

Aufarbeitung

  1. filtrationThe catalyst is filtered off
  2. customthe filtrate is evaporated
  3. extractionThe separated oil is extracted with chloroform
  4. dry with materialthe chloroform solution is dried over sodium sulphate
  5. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-f3f0daef5bb3420fb5df1f9d4d60a4da
Quelldatensatz
uspto-grants-1984_08
Patentnummer
US04465855

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