Реакция #2320132

ord-e80a3a72b5aa4bd3ac30a1d4ea6c7a3c

Уравнение реакции

CCOCCO
2-ethoxyethanol
Cc1ccccc1-c1cccc(-c2ccccn2)c1
2-(2′-methylbiphenyl-3-yl)pyridine
Cc1ccc(-c2cccc(-c3ccccc3C)c2)nc1
2-(2′-methylbiphenyl-3-yl)5-methylpyridine

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe reaction mixture was heated under a nitrogen atmosphere
  2. 2
    Температураat reflux for 50 h
  3. 3
    Температураcooled
  4. 4
    ДругоеThe yellow precipitate that formed
  5. 5
    Фильтрацияwas collected by vacuum filtration
  6. 6
    Промывкаwashed with methanol and ethyl acetate
  7. 7
    Другоеto give 11.0 g (70%) of chloro-bridged dimer

Методика

To a mixture of 2-ethoxyethanol (95 mL) and water (25 mL) were added 11.0 g (42.4 mmol) of 2-(2′-methylbiphenyl-3-yl)pyridine and 7.9 g (21.2 mmol) of IrCl3. The reaction mixture was heated under a nitrogen atmosphere at reflux for 50 h and cooled. The yellow precipitate that formed was collected by vacuum filtration and washed with methanol and ethyl acetate to give 11.0 g (70%) of chloro-bridged dimer

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07709100B2uspto-grants-2010_05