تفاعل #2146688
ord-70504a38808348daa5aae6cbbda8ff2d
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.DISTILLATIONto distill off methanol
- 2درجة الحرارةAfter the reaction solution was cooled down to 5° 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
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).