HRID2040444

反应详情

EQUATION

反应方程式

HRID 2040444 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

A 1.7 M solution of tert-butyllithium in pentane (57.8 mL) was added to THF (200 ml) at −78° C. 2-Bromomesitylene (3.6 mL) was added dropwise, keeping the temperature below −60° C., and the mixture stirred at −78° C. for 1 h. 3-Methoxypyridine (3.6 mL) was added dropwise at −78° C. and then the mixture was allowed to warm to −5° C. over 2 h. The reaction mixture was re-cooled to −78° C. and a slurry of 5-chloroisatin (3.26 g) in THF (100 mL) was added portionwise keeping the temperature below −60° C. The reaction mixture was stirred at −78° C. for 1 h. The cooling bath was removed and the reaction mixture was stirred for 30 min. The reaction mixture was quenched with 10% aqueous ammonium chloride solution and extracted several times with ethyl acetate. The combined organic layers were washed with water, dried over magnesium sulfate and evaporated to low volume. Upon standing, 0.73 g of a pale yellow solid separated which was filtered off, washed with ethyl acetate and dried in vacuo.

WORKUP

后处理

  1. customthe temperature below −60° C.
  2. temperatureto warm to −5° C. over 2 h
  3. temperatureThe reaction mixture was re-cooled to −78° C.
  4. customthe temperature below −60° C
  5. stirringThe reaction mixture was stirred at −78° C. for 1 h
  6. customThe cooling bath was removed
  7. stirringthe reaction mixture was stirred for 30 min
  8. customThe reaction mixture was quenched with 10% aqueous ammonium chloride solution
  9. extractionextracted several times with ethyl acetate
  10. washThe combined organic layers were washed with water
  11. dry with materialdried over magnesium sulfate
  12. customevaporated to low volume
  13. custom0.73 g of a pale yellow solid separated which
  14. filtrationwas filtered off
  15. washwashed with ethyl acetate
  16. customdried in vacuo