HRID381835

反应详情

EQUATION

反应方程式

HRID 381835 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a stirred mixture of (4-methylphenyl)boronic acid (0.818 g, 0.00602 mol) and 4-(4-bromo-phenyl)-4-oxo-butyric acid, methyl ester (1.3556 g, 0.00500 mol) in toluene (10 mL) was added tetrakis(triphenylphosphine)-palladium(0) (0.173 g, 0.000150 mol) and 2.0 M aqueous sodium carbonate (5.0 mL, 0.010 mol), and the mixture was heated at reflux under nitrogen for 12 hours and allowed to cool. The mixture was diluted with toluene and dichloromethane (10 mL/10 mL), and filtered through a pad of Celite. The Celite was washed with additional toluene and dichloromethane. Filtrate and washings were combined and washed with 2.0 M aqueous sodium carbonate, brine, 3% aqueous ammonium hydroxide, water, and brine. The organics were dried (Na2SO4) and rotary evaporated. The residue was dissolved in chloroform and purified by column chromatography on silica gel (144 g, 230-400 mesh), eluting with hexanes-acetone (6:1, 17×125 mL) to give 0.98 g of 4-(4′-methyl-biphenyl-4-yl)-4-oxo-butyric acid, methyl ester as a white solid; mp 121-122° C.

WORKUP

后处理

  1. temperaturethe mixture was heated
  2. temperatureat reflux under nitrogen for 12 hours
  3. temperatureto cool
  4. filtrationfiltered through a pad of Celite
  5. washThe Celite was washed with additional toluene and dichloromethane
  6. washwashed with 2.0 M aqueous sodium carbonate, brine, 3% aqueous ammonium hydroxide, water, and brine
  7. dry with materialThe organics were dried (Na2SO4) and rotary evaporated
  8. dissolutionThe residue was dissolved in chloroform
  9. custompurified by column chromatography on silica gel (144 g, 230-400 mesh)
  10. washeluting with hexanes-acetone (6:1, 17×125 mL)