HRID440338

反应详情

EQUATION

反应方程式

HRID 440338 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

2-(9-Fluorenyl) ethanol was prepared from a solution of fluorene (116.35 g, 0.7 mmol) in 800 ml of dry THF at -20° C. which was added n-Buli in hexane (0.7 mol) keeping the temperature below -10° C. To the clear solution was rapidly added 357 ml of 1.4M ethylene oxide in ether (0.5 mol) keeping the temperature below 5° C. The reaction mixture was stirred for 5 hours, then quenched with 50 ml of saturated ammonium chloride solution. The THF was removed at a rotary evaporator. The residue was partitioned between water and ethyl acetate. The organic layer was separated, dried with MgSO4 and concentrated in vacuo until crystallization began. The solution was allowed to stand overnight and the crystals were collected and dried (mp 97° C.) (85.5 g, (81%)).

WORKUP

后处理

  1. customthe temperature below -10° C
  2. customthe temperature below 5° C
  3. customquenched with 50 ml of saturated ammonium chloride solution
  4. customThe THF was removed at a rotary evaporator
  5. customThe residue was partitioned between water and ethyl acetate
  6. customThe organic layer was separated
  7. dry with materialdried with MgSO4
  8. concentrationconcentrated in vacuo until crystallization
  9. waitto stand overnight
  10. customthe crystals were collected
  11. customdried (mp 97° C.) (85.5 g, (81%))