Реакция #55985

ord-c4eb971eb70b4c42af88f7786086da5f

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураcooling
  2. 2
    Другоеto come to RT
  3. 3
    workup.ADDITION41 g of aluminumtrichloride (310 mmol) is added in portions over a 3 hour period with ice bath
  4. 4
    Температураcooling
  5. 5
    ТемператураThe solution is heated to 25° for 1 hour
  6. 6
    Температураheated
  7. 7
    Температураto reflux for 2 hours
  8. 8
    Температураfinally cooled
  9. 9
    workup.STIRRINGstirred overnight
  10. 10
    workup.ADDITIONThe mixture is poured onto ice/conc
  11. 11
    ПромывкаHCl, then washed with ether
  12. 12
    workup.ADDITIONFifty Percent (50%) sodium hydroxide is added until the precipitate
  13. 13
    workup.DISSOLUTIONis dissolved
  14. 14
    ЭкстракцияThe solution is extracted with CHCl3
  15. 15
    Промывкаwashed with water
  16. 16
    Другоеdried

Методика

To 15 g of 6-methyl-2-pyridylcarboxylic acid (122 mmol) in 200 ml benzene is added dropwise 19.1 g (150 mmol) oxalyl chloride (dissolved in 30 ml benzene) with ice bath cooling. The solution is allowed to come to RT and is stirred 1 hour, after which it is stripped, 100 ml of benzene is added, and it is stripped again. The residue is taken up in 200 ml benzene and 41 g of aluminumtrichloride (310 mmol) is added in portions over a 3 hour period with ice bath cooling. The solution is heated to 25° for 1 hour, then heated to reflux for 2 hours, and finally cooled and stirred overnight. The mixture is poured onto ice/conc. HCl, then washed with ether. Fifty Percent (50%) sodium hydroxide is added until the precipitate is dissolved. The solution is extracted with CHCl3, washed with water, dried and stripped, leaving 6-benzoyl-2-methylpyridine.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04223033uspto-grants-1980_09