تفاعل #2146683
ord-d3d3991aa5a44e8db26544bd16e548a1
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.DISTILLATIONto distill off methanol
- 2درجة الحرارةAfter the reaction solution was cooled down to 10° C.
- 3أخرىAfter the completion of the reaction
- 4استخلاصextracted twice with chloroform
- 5غسيلThe combined chloroform layer was washed with a 1 mol/L sodium hydroxide solution
- 6غسيلwashed twice with a saturated sodium chloride solution
- 7تجفيفdried over anhydrous sodium sulfate
- 8workup.DISTILLATIONAfter the solvent was distilled off under reduced pressure
الإجراء التجريبي
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).