反应 #2146683

ord-d3d3991aa5a44e8db26544bd16e548a1

反应方程式

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

反应条件

温度
90°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.DISTILLATIONto distill off methanol
  2. 2
    温度After the reaction solution was cooled down to 10° C.
  3. 3
    其他After the completion of the reaction
  4. 4
    萃取extracted twice with chloroform
  5. 5
    洗涤The combined chloroform layer was washed with a 1 mol/L sodium hydroxide solution
  6. 6
    洗涤washed twice with a saturated sodium chloride solution
  7. 7
    干燥dried over anhydrous sodium sulfate
  8. 8
    workup.DISTILLATIONAfter the solvent was distilled off under reduced pressure

实验过程

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).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08277777B2uspto-grants-2012_10