تفاعل #2146688

ord-70504a38808348daa5aae6cbbda8ff2d

معادلة التفاعل

CO.C[O-].[Na+]
sodium methoxide methanol
Oc1cccnc1Br
2-bromo-3-hydroxypyridine
CI
methyl iodide
COc1cccnc1Br
2-bromo-3-methoxypyridine

المذيبات

ظروف التفاعل

درجة الحرارة
90°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.DISTILLATIONto distill off methanol
  2. 2
    درجة الحرارةAfter the reaction solution was cooled down to 5° C.
  3. 3
    أخرىAfter the completion of the reaction
  4. 4
    استخلاصextracted twice with chloroform
  5. 5
    غسيلThe combined chloroform layer was washed with a 1 mol/L sodium hydroxide solution
  6. 6
    غسيلwashed twice with a saturated sodium chloride solution
  7. 7
    تجفيفdried over anhydrous sodium sulfate
  8. 8
    workup.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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08277777B2uspto-grants-2012_10