Reaktion #77948

Reaktionsgleichung

3-(3-bromo-2-methyl-6-methylsulfonylphenyl)-4,5-dihydroisoxazole

1-methyl-5-hydroxypyrazole

potassium carbonate

triethylamine

triphenylphosphine

1,4-dioxane

→

1-Methyl-4-(3-(4,5-dihydroisoxazol-3-yl)-2-methyl-4-methyl -sulfonylbenzoyl)-5-hydroxypyrazole

Reaktionsbedingungen

Aufarbeitung

1. 1
   WaschenThe autoclave was washed twice with nitrogen
2. 2
   Temperaturthe mixture was heated
3. 3
   workup.ADDITIONBy continuous addition of carbon monoxide
4. 4
   workup.STIRRINGthe mixture was stirred at 130° C. for 36 h
5. 5
   Filtrationthe precipitated palladium was filtered off over a blue-band filter (pore size 2 to 3 μ)
6. 6
   Waschenwashed with water
7. 7
   workup.DISTILLATIONDioxane, triethylamine and some of the water were then distilled off in one step (150 mbar or atmospheric pressure)
8. 8
   workup.STIRRINGstirred at 5° C. for 12 h, while the pH
9. 9
   FiltrationThe precipitate was filtered off
10. 10
    Waschenwashed three times with water
11. 11
    Sonstigedried at 70° C. under reduced pressure

Vorschrift

2 l of 1,4-dioxane, 250 g (0.77 mol) of 3-(3-bromo-2-methyl-6-methylsulfonylphenyl)-4,5-dihydroisoxazole, 77 g (0.77 mol) of 1-methyl-5-hydroxypyrazole, 269 g (1.93 mol) of potassium carbonate, 197 g (1.93 mol) of triethylamine, 1.39 g (0.0077 mol) of palladium(II) chloride and 4.12 g (0.0154 mol) of triphenylphosphine were added to a 3.5 l autoclave. The autoclave was washed twice with nitrogen, the mixture was heated with stirring to 130° C. and a carbon monoxide pressure of 6 kg/cm2 was applied. By continuous addition of carbon monoxide, the carbon monoxide pressure was kept constant at 6 kg/cm2 and the mixture was stirred at 130° C. for 36 h. The mixture was then admixed with 1 l of demineralized water and the precipitated palladium was filtered off over a blue-band filter (pore size 2 to 3 μ) and washed with water. Dioxane, triethylamine and some of the water were then distilled off in one step (150 mbar or atmospheric pressure). The aqueous phase was adjusted to pH 2.5 using 20% strength sulfuric acid and stirred at 5° C. for 12 h, while the pH was being readjusted. The precipitate was filtered off, washed three times with water and dried at 70° C. under reduced pressure. This gave 227 g of product (calc. 100%).

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