Реакция #487564

ord-2b6c5141eef649918800f0a6fff9105f

Уравнение реакции

CCc1ccc(Br)cc1C1C(=O)CCC(C)(C)C1=O
2-(5-bromo-2-ethylphenyl)-4,4-dimethylcyclohexane-1,3-dione
Cc1cc(Cl)ccc1B(O)O
2-methyl-4-chloro-phenylboronic acid
[Cs+].[F-]
cesium fluoride
CCc1ccc(-c2ccc(Cl)cc2C)cc1C1C(=O)CCC(C)(C)C1=O
2-(4′-chloro-4-ethyl-2′-methylbiphen-3-yl)-4,4-dimethyl-cyclohexane-1,3-dione

Растворители

Условия реакции

Температура
80°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe warm reaction mixture
  2. 2
    Фильтрацияis filtered
  3. 3
    Промывкаwashing the filter cake with 9:1 dichloromethane
  4. 4
    КонцентрированиеThe mixture is concentrated under reduced pressure
  5. 5
    Другоеthe residue is purified by column chromatography on silica gel

Методика

A mixture of 2-(5-bromo-2-ethylphenyl)-4,4-dimethylcyclohexane-1,3-dione (0.194 g, 0.6 mmol), 2-methyl-4-chloro-phenylboronic acid (0.153 g, 0.9 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (complex with dichloromethane 1:1) (80 mg, 0.098 mmol) and cesium fluoride (0.608 g, 4 mmol) are stirred together in 1,2-dimethoxyethane (4 ml) and the reaction mixture is heated at 80° C. overnight. The warm reaction mixture is filtered, washing the filter cake with 9:1 dichloromethane:methanol. The mixture is concentrated under reduced pressure and the residue is purified by column chromatography on silica gel to give 2-(4′-chloro-4-ethyl-2′-methylbiphen-3-yl)-4,4-dimethyl-cyclohexane-1,3-dione.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08741806B2uspto-grants-2014_06