3,5-Dibromopyridine → 3-Bromo-5-methoxypyridine

HRID 1828938Notes

Reaction equation

HRID 1828938 reaction equation
[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6](Br)[CH:7]=1.[CH3:9][O-:10].[Na+]>CO.[Cu]>[Br:1][C:2]1[CH:7]=[C:6]([O:10][CH3:9])[CH:5]=[N:4][CH:3]=1

Participants

5

Conditions

Temperature
150 °C

Procedure

A mixture of 3,5-dibromopyridine (20.00 g, 84.42 mmol), sodium methoxide (11.40 g, 211.06 mmol), and copper powder (1 g, 5% by weight of 3,5-dibromopyridine) in dry methanol was heated in a sealed glass tube at 150° C. for 14 h. The reaction mixture was cooled to ambient temperature and extracted with diethyl ether (4×200 mL). The combined ether extracts were dried over sodium sulfate, filtered, and concentrated by rotary evaporation. The crude product was purified by column chromatography over aluminum oxide, eluting with ethyl acetate-hexane (1:9, v/v). Selected fractions were combined and concentrated by rotary evaporation, producing 9.40 g (59.5%) of a colorless oil, which tended to crystallize upon cooling.

Workup

  1. temperatureThe reaction mixture was cooled to ambient temperature
  2. extractionextracted with diethyl ether (4×200 mL)
  3. dry with materialThe combined ether extracts were dried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated by rotary evaporation
  6. customThe crude product was purified by column chromatography over aluminum oxide
  7. washeluting with ethyl acetate-hexane (1:9, v/v)
  8. concentrationconcentrated by rotary evaporation

Sources & evidence

ORD record
ord-7aa09a0ba66f4b17883505d21b5c35c7
Source dataset
uspto-grants-2006_06
Patent number
US07060826B2

Reaction notes

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