2,6-Dibromopyridine → 2-Bromo-6-methoxypyridine

HRID 1359263Notes

Reaction equation

HRID 1359263 reaction equation
[CH3:1][OH:2].C[O-].[Na+].[Br:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9](Br)[N:8]=1>CO>[Br:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([O:2][CH3:1])[N:8]=1

Participants

4

Conditions

Temperature
80 °C

Procedure

250 ml of 28% sodium methoxide methanol solution was added dropwise into a mixture of 200 g of 2,6-dibromopyridine and 150 ml of methanol while heating at 80° C. stirring in an oil bath, followed by stirring under heating for 2 hours as it was. After cooling as it was, the mixture was extracted with diethyl ether-water, and the organic phase was washed with water and brine, dried over anhydrous magnesium sulfate and the solvent was removed, to give 150 g of the target compound.

Workup

  1. stirringby stirring
  2. temperatureunder heating for 2 hours as it
  3. temperatureAfter cooling as it
  4. extractionthe mixture was extracted with diethyl ether-water
  5. washthe organic phase was washed with water and brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customthe solvent was removed

Sources & evidence

ORD record
ord-19ae1b4156a448a0ab5bd25fbab2cc5b
Source dataset
uspto-grants-2003_07
Patent number
US06599917B1

Reaction notes

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