Reaktion #2389080

Reaktionsgleichung

4-(5-bromo-6-methoxy-2-naphthyl)-4-hydroxybut-3-en-2-one

hydrogen

sodium acetate

→

nabumetone

Lösungsmittel

water

isopropanol

isopropanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   WaschenThe hydrogenator is washed with nitrogen in order
2. 2
   workup.ADDITIONhydrogen is introduced at the pressure of 2.5 atmospheres
3. 3
   SonstigeFor a period of time of 9 hours the temperature of reaction
4. 4
   Sonstigeis kept at 50° C.
5. 5
   Waschenthe hydrogenator is washed with nitrogen
6. 6
   Filtrationthe reaction mixture is filtered in order
7. 7
   EinengenThe solution is concentrated to 130 ml
8. 8
   workup.ADDITIONdiluted with 45 ml of water
9. 9
   workup.ADDITIONadded with 18.2 g of sodium metabisulfite
10. 10
    Temperaturis cooled to 0° C
11. 11
    SonstigeThe so obtained suspension
12. 12
    workup.WAITis kept at 0° C. for two hours
13. 13
    Filtrationis filtered
14. 14
    Waschenthe solid is washed with 60 ml of isopropanol
15. 15
    Temperaturcooled to 0° C.
16. 16
    Temperaturhalf at room temperature, then is heated at 60° C.
17. 17
    Sonstigethe layers are separated
18. 18
    WaschenThe organic phase is washed with 60 ml of water
19. 19
    Einengenis concentrated under vacuum at 60° C. until an oil
20. 20
    Sonstigeis obtained which
21. 21
    Temperaturby cooling
22. 22
    Temperaturthe resulting solution is cooled to 0° C. in two hours
23. 23
    workup.WAITThe obtained suspension is kept for one hour at this temperature
24. 24
    Filtrationfiltered
25. 25
    Waschenwashed with 10 ml of cold isopropanol
26. 26
    Sonstigedried in oven under vacuum until constant weight

Vorschrift

49.44 Grams (0.154 moles) of 4-(5-bromo-6-methoxy-2-naphthyl)-4-hydroxybut-3-en-2-one, 12.24 g (0.149 moles) of anhydrous sodium acetate, 4 g of a 50% suspension in water of 5% palladium on carbon, equivalent to 0.00094 moles of palladium and 400 ml of isopropanol are put into a hydrogenator. The hydrogenator is washed with nitrogen in order to eliminate the oxygen and then hydrogen is introduced at the pressure of 2.5 atmospheres. For a period of time of 9 hours the temperature of reaction is kept at 50° C., then the hydrogen is let off, the hydrogenator is washed with nitrogen and the reaction mixture is filtered in order to eliminate the catalyst. The solution is concentrated to 130 ml, diluted with 45 ml of water, heated to 60° C. and added with 18.2 g of sodium metabisulfite. The reaction mixture is kept for one hour at 60° C. and then is cooled to 0° C. The so obtained suspension is kept at 0° C. for two hours and then is filtered; the solid is washed with 60 ml of isopropanol cooled to 0° C. and then is suspended in a mixture made by 70 ml of a 10% aqueous solution of sodium hydroxide and 270 ml of toluene. The reaction mixture is stirred for one hour and half at room temperature, then is heated at 60° C. and the layers are separated. The organic phase is washed with 60 ml of water and is concentrated under vacuum at 60° C. until an oil is obtained which solidifies by cooling. The solid is dissolved at 60° C. in 40 ml of isopropanol and the resulting solution is cooled to 0° C. in two hours. The obtained suspension is kept for one hour at this temperature, filtered, washed with 10 ml of cold isopropanol and dried in oven under vacuum until constant weight. 26.3 Grams of nabumetone are obtained with a yield equal to 74.8%.

Quelle