HRID1369628

反应详情

EQUATION

反应方程式

HRID 1369628 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-10 °C

PROCEDURE

实验过程

To a stirred solution of dilsopropylamine (4.5 mL, 31.78 mmol) in anhydrous tetrahydrofuiran (20 mL) under nitrogen atmosphere at −5° C. was added dropwise n-BuLi in hexanes (2.5 M solution, 12.8 mL, 31.78 mmol) maintaining internal temperature of the reaction mixture below 0° C. The reaction mixture was stirred at −10° C. for 10 minutes, then at 0° C. for 30 minutes. This was cooled to −78° C. and a solution of Example 236A (5.8 g, 26.5 mmol) in anhydrous tetrahydroffiran (30 mL) was added slowly. Stirring at −78° C. was continued for 1 hour. Then the reaction was quenched with dropwise addition of methyl formate (5 mL, 79.5 mmol) in anhydrous THF (15 mL) and stirred at −78° C. for 3.5 hours. Internal temperature of the reaction mixture was maintained at or below −74° C. throughout the reaction. After 3.5 hours, the reaction mixture was poured into an ice cold saturated aqueous solution of NaHCO3 (200 mL) and stirred for 15 minutes. The mixture was partitioned with ethyl acetate (250 mL), organic layer was separated and washed with brine (2×60 mL). The dried (MgSO4) organic layer was concentrated under reduced pressure to obtain the crude product (8.5 g). The title compound was obtained in 75% yield (4.2 g) by flash chromatography on silica gel eluting with 6% acetone-hexane.

WORKUP

后处理

  1. temperaturemaintaining internal temperature of the reaction mixture below 0° C
  2. waitat 0° C. for 30 minutes
  3. temperatureThis was cooled to −78° C.
  4. stirringStirring at −78° C.
  5. waitwas continued for 1 hour
  6. stirringstirred at −78° C. for 3.5 hours
  7. temperatureInternal temperature of the reaction mixture was maintained at or below −74° C.
  8. customthroughout the reaction
  9. waitAfter 3.5 hours
  10. stirringstirred for 15 minutes
  11. customThe mixture was partitioned with ethyl acetate (250 mL), organic layer
  12. customwas separated
  13. washwashed with brine (2×60 mL)
  14. dry with materialThe dried (MgSO4) organic layer
  15. concentrationwas concentrated under reduced pressure
  16. customto obtain the crude product (8.5 g)