Reacción #532291

Ecuación de reacción

ammonium chloride

5-bromo-2-hydroxy-4-methylpyridine

sodium hydride

3-hydroxy-3-methylbutyl 4-methylbenzene sulfonate

→

compound

Rendimiento 63.1%

4-(5-bromo-4-methylpyridin-2-yloxy)-2-methylbutan-2-ol

Rendimiento 63.1%

Disolventes

N,N-dimethylformamide

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONwas added
2. 2
   Temperaturacooling
3. 3
   Otrothe resultant reaction mixture
4. 4
   Otrothe resultant reaction mixture
5. 5
   workup.STIRRINGwas stirred at 60° C. for 4 hours
6. 6
   Otrothe resultant reaction mixture
7. 7
   Extracciónwas extracted with ethyl acetate
8. 8
   LavadoThe organic phase was washed with saturated saline
9. 9
   Secadowas dried over anhydrous sodium sulfate
10. 10
    workup.DISTILLATIONFrom the organic phase, the solvent was distilled off under reduced pressure
11. 11
    Otrothe resultant residue was purified by silica gel column chromatography (eluate; n-hexane:ethyl acetate=50:50 to 33:67)

Procedimiento

To a suspension of sodium hydride (to which about 40% of a mineral oil was added, 0.23 g) in N,N-dimethylformamide (10 mL), 5-bromo-2-hydroxy-4-methylpyridine (1.00 g) was added under ice-cooling and the resultant reaction mixture was stirred for 30 minutes. To the reaction mixture, 3-hydroxy-3-methylbutyl 4-methylbenzene sulfonate (1.51 g) was added and the resultant reaction mixture was stirred at 60° C. for 4 hours. To the reaction mixture, a aqueous solution of saturated ammonium chloride was added and the resultant reaction mixture was extracted with ethyl acetate. The organic phase was washed with saturated saline and was dried over anhydrous sodium sulfate. From the organic phase, the solvent was distilled off under reduced pressure and the resultant residue was purified by silica gel column chromatography (eluate; n-hexane:ethyl acetate=50:50 to 33:67) to obtain the subject compound (0.92 g) as a light yellow oil.

Fuente