HRID270152

反应详情

EQUATION

反应方程式

HRID 270152 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a 500ml round-bottom flask equipped with a magnetic stir-bar was mixed ethyl 4-{[tert-butyl(diphenyl)silyl]oxy}-2-chloro-3-oxobutanoate (20.4g, 52.88mmoles, 1eq), 4-trifluoromethylthiobenzamide (12.2g, 59.5mmoles, 1.1eq), 1,2-dichloroethane (150ml, 0.44M) and H2O (3ml). This mixture was refluxed for 12hrs. After cooling to room temperature, the reaction mixture was diluted with CH2Cl2(100ml) and washed with sat. NaHCO3. Once the phases were separated, the organic phase washed with water, brine and dried over Na2SO4. This was then filtered, concentrated in vacuo and purified via silica gel chromatography (5% EtOAc/Hexanes to 20% EtOAc/Hexanes) to yield 20.3g (76%) of the titled compound.

WORKUP

后处理

  1. customTo a 500ml round-bottom flask equipped with a magnetic stir-bar
  2. temperatureThis mixture was refluxed for 12hrs
  3. washwashed with sat. NaHCO3
  4. customOnce the phases were separated
  5. washthe organic phase washed with water, brine
  6. dry with materialdried over Na2SO4
  7. filtrationThis was then filtered
  8. concentrationconcentrated in vacuo
  9. custompurified via silica gel chromatography (5% EtOAc/Hexanes to 20% EtOAc/Hexanes)