تفاعل #2146683

ord-d3d3991aa5a44e8db26544bd16e548a1

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 10° 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

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).

المصدر

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