Réaction #2146683

Équation de réaction

sodium methoxide methanol

2-bromo-3-hydroxypyridine

methyl iodide

→

2-bromo-3-methoxypyridine

Solvants

dimethylsulfoxide

Conditions de réaction

Traitement

1. 1
   workup.DISTILLATIONto distill off methanol
2. 2
   TempératureAfter the reaction solution was cooled down to 10° C.
3. 3
   AutreAfter the completion of the reaction
4. 4
   Extractionextracted twice with chloroform
5. 5
   LavageThe combined chloroform layer was washed with a 1 mol/L sodium hydroxide solution
6. 6
   Lavagewashed twice with a saturated sodium chloride solution
7. 7
   Séchagedried over anhydrous sodium sulfate
8. 8
   workup.DISTILLATIONAfter the solvent was distilled off under reduced pressure

Mode opératoire

100.0 g (corresponding to 0.575 mol) of 2-bromo-3-hydroxypyridine was dissolved in 310 mL of dimethylsulfoxide, and 575 mL (corresponding to 0.575 mol) 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 10° C. or lower, 93.9 g (corresponding to 0.662 mol) of methyl iodide was added, and then stirred at room temperature for 20.5 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, 65.4 g (corresponding to 0.348 mol) of 2-bromo-3-methoxypyridine was obtained (FIG. 2, Step 1).

Source