HRID265646

反应详情

EQUATION

反应方程式

HRID 265646 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

To 3-chlorothiophene (5.0 g, 42.16 mmol), dissolved in 50 mL of tetrahydrofuran stirring at -72° C. (acetone/dry ice bath), was added 16.8 ml of 2.5M hexane solution of n-butyllithium over a 15 minute period. The reaction temperature was maintained below -70° C. during the addition. Soon after complete addition of the n-butyllithium a white precipitate formed. After 40 minutes of stirring below -70° C., 5.88 mL of chlorotrimethylsilane was slowly added over a 5 minute period. After addition the solution momentarily became clear before turning cloudy again by the formation of lithium chloride by-product. After 10 minutes the reaction solution was warmed to 0° C. At 0° C. 5 mL of water followed by 25 mL of brine was added to quench the reaction. The aqueous solution was then extracted with ethyl acetate (2×30 mL). The organic extract was dried (Na2SO4), filtered and evaporated to 8.0 g of title compound as a clear oil.

WORKUP

后处理

  1. temperatureThe reaction temperature was maintained below -70° C. during the addition
  2. customformed
  3. additionAfter addition the solution momentarily became clear
  4. customAt 0° C
  5. additionwas added
  6. customto quench
  7. customthe reaction
  8. extractionThe aqueous solution was then extracted with ethyl acetate (2×30 mL)
  9. extractionThe organic extract
  10. dry with materialwas dried (Na2SO4)
  11. filtrationfiltered
  12. customevaporated to 8.0 g of title compound as a clear oil