Reacción #2146688

Ecuación de reacción

sodium methoxide methanol

2-bromo-3-hydroxypyridine

methyl iodide

→

2-bromo-3-methoxypyridine

Disolventes

dimethylsulfoxide

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.DISTILLATIONto distill off methanol
2. 2
   TemperaturaAfter the reaction solution was cooled down to 5° C.
3. 3
   OtroAfter the completion of the reaction
4. 4
   Extracciónextracted twice with chloroform
5. 5
   LavadoThe combined chloroform layer was washed with a 1 mol/L sodium hydroxide solution
6. 6
   Lavadowashed twice with a saturated sodium chloride solution
7. 7
   Secadodried over anhydrous sodium sulfate
8. 8
   workup.DISTILLATIONAfter the solvent was distilled off under reduced pressure

Procedimiento

31.11 g (corresponding to 178.88 mmol) of 2-bromo-3-hydroxypyridine was dissolved in 95.8 mL of dimethylsulfoxide, and 89.9 mL (corresponding to 89.9 mmol) of a 1 mol/L sodium methoxide-methanol solution was added thereto. Then, the reaction solution was heated to 90° C. to distill off methanol. After the reaction solution was cooled down to 5° C. or lower, 29.2 g (corresponding to 205.62 mmol) of methyl iodide was added, and then stirred at room temperature for 17 hours. After the completion of the reaction, the reaction solution was poured into ice-water and extracted twice with chloroform. The combined chloroform layer was washed with a 1 mol/L sodium hydroxide solution, washed twice with a saturated sodium chloride solution, and dried over anhydrous sodium sulfate. After the solvent was distilled off under reduced pressure, 20.74 g (corresponding to 110.31 mmol) of 2-bromo-3-methoxypyridine was obtained (FIG. 3, Step 1).

Fuente