HRID1454081

反应详情

EQUATION

反应方程式

HRID 1454081 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-5 °C

PROCEDURE

实验过程

A suspension of (3,3,3-trifluoropropyl)triphenylphosphonium iodide (194.5 g, 0.4 moles) in tetrahydrofuran (THF—anhydrous, 800 mL) was cooled to −5° C. in an ice/brine bath under nitrogen. Lithium bis(trimethylsilyl)amide (1.0 M in THF, 800 mL, 0.8 moles) was added to this suspension drop-wise over 2 hours. The temperature was maintained below 5° C. throughout the addition. The reaction mixture was then cooled to −75° C. in a dry ice/acetone bath. To this solution, ethylchloroformate (76.5 mL, 0.8 moles) was added drop-wise over 30 minutes. The reaction was stirred at −75° C. for an additional hour and allowed to warm to 25° C. overnight. The reaction mixture was poured onto brine (1.5 L) and stirred for 30 minutes. The layers were separated and the organic layer was washed with brine (200 mL). The aqueous layer was washed with dichloromethane (CH2Cl2−2×200 mL) and the combined organics were concentrated to a residue. This residue was redissolved in CH2Cl2 (500 mL), dried over MgSO4, and filtered through a plug of magnasol. The solvent was reduced to a minimum (˜100 mL) in vacuo and the product was precipitated with hexanes (250 mL). The solvent was completely removed in vacuo and the solid product was triturated with hexanes (500 mL). The solid was isolated by filtration and dried overnight in vacuo at 25° C. to give a beige powder 152.8 g, 89%).

WORKUP

后处理

  1. temperatureThe temperature was maintained below 5° C. throughout the addition
  2. temperatureThe reaction mixture was then cooled to −75° C. in a dry ice/acetone bath
  3. temperatureto warm to 25° C. overnight
  4. additionThe reaction mixture was poured onto brine (1.5 L)
  5. stirringstirred for 30 minutes
  6. customThe layers were separated
  7. washthe organic layer was washed with brine (200 mL)
  8. washThe aqueous layer was washed with dichloromethane (CH2Cl2−2×200 mL)
  9. concentrationthe combined organics were concentrated to a residue
  10. dissolutionThis residue was redissolved in CH2Cl2 (500 mL)
  11. dry with materialdried over MgSO4
  12. filtrationfiltered through a plug of magnasol
  13. customthe product was precipitated with hexanes (250 mL)
  14. customThe solvent was completely removed in vacuo
  15. customthe solid product was triturated with hexanes (500 mL)
  16. customThe solid was isolated by filtration
  17. customdried overnight in vacuo at 25° C.