HRID41674

反应详情

EQUATION

反应方程式

HRID 41674 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

To a solution of 3,5-dibromo-2-ethyl-thiophene (3.28 g, 12.15 mmol) in diethyl ether (50 ml) at −78° C. under N2 is added, slowly, 2.5M butyl lithium in hexane solution (4.86 ml, 12.15 mmol) over 10 minutes and the reaction stirred at −78° C. for a further 30 minutes. The reaction is then cooled to −78° C. before the dropwise addition of trimethyl borate (1.64 ml, 14.6 mmol) over 5 minutes. The reaction is stirred at −78° C. for 30 minutes, then allowed to warm to room temperature and stirred for a further 60 minutes. Palladium acetate (68 mg, 0.3 mmol), triphenylphosphine (314 mg, 1.2 mmol) and 4-chloro-iodobenzene (4.9 g, 12.15 mmol) is then added to the reaction, followed by THF (50 ml) and 1N sodium carbonate solution (20 ml) and the reaction is heated to reflux for 3 hours. The cooled reaction mixture is partitioned between ether (250 ml) and water (300 ml). The organic layer is separated, dried over magnesium sulphate, filtered and evaporated under reduced pressure. The residue is therefore purified by flash chromatography on silica gel to give 3-bromo-5-(4-chlorophenyl)-2-ethyl-thiophene as a white solid (2.75 g).

WORKUP

后处理

  1. stirringThe reaction is stirred at −78° C. for 30 minutes
  2. temperatureto warm to room temperature
  3. stirringstirred for a further 60 minutes
  4. temperaturethe reaction is heated
  5. temperatureto reflux for 3 hours
  6. customThe cooled reaction mixture
  7. customis partitioned between ether (250 ml) and water (300 ml)
  8. customThe organic layer is separated
  9. dry with materialdried over magnesium sulphate
  10. filtrationfiltered
  11. customevaporated under reduced pressure
  12. customThe residue is therefore purified by flash chromatography on silica gel