Reacción #2389080

ord-8201d360a54a443daad22402d726eea2

Ecuación de reacción

COc1ccc2cc(C(O)=CC(C)=O)ccc2c1Br
4-(5-bromo-6-methoxy-2-naphthyl)-4-hydroxybut-3-en-2-one
[H][H]
hydrogen
CC(=O)[O-].[Na+]
sodium acetate
COc1ccc2cc(CCC(C)=O)ccc2c1
nabumetone

Condiciones de reacción

Temperatura
60°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    LavadoThe hydrogenator is washed with nitrogen in order
  2. 2
    workup.ADDITIONhydrogen is introduced at the pressure of 2.5 atmospheres
  3. 3
    OtroFor a period of time of 9 hours the temperature of reaction
  4. 4
    Otrois kept at 50° C.
  5. 5
    Lavadothe hydrogenator is washed with nitrogen
  6. 6
    Filtraciónthe reaction mixture is filtered in order
  7. 7
    ConcentraciónThe 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
    Temperaturais cooled to 0° C
  11. 11
    OtroThe so obtained suspension
  12. 12
    workup.WAITis kept at 0° C. for two hours
  13. 13
    Filtraciónis filtered
  14. 14
    Lavadothe solid is washed with 60 ml of isopropanol
  15. 15
    Temperaturacooled to 0° C.
  16. 16
    Temperaturahalf at room temperature, then is heated at 60° C.
  17. 17
    Otrothe layers are separated
  18. 18
    LavadoThe organic phase is washed with 60 ml of water
  19. 19
    Concentraciónis concentrated under vacuum at 60° C. until an oil
  20. 20
    Otrois obtained which
  21. 21
    Temperaturaby cooling
  22. 22
    Temperaturathe 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
    Filtraciónfiltered
  25. 25
    Lavadowashed with 10 ml of cold isopropanol
  26. 26
    Otrodried in oven under vacuum until constant weight

Procedimiento

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%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE037813E1uspto-grants-2002_08