反应 #1148658

ord-c67773a842d44d21a64959c4b7aa354a

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度then cooled to 0° C
  2. 2
    温度to warm to room temperature overnight
  3. 3
    其他After quenching with saturated aqueous NH4Cl
  4. 4
    其他the resulting layers were separated
  5. 5
    萃取the aqueous layer was extracted with Et2O (2×)
  6. 6
    干燥The combined organic layers were dried over Na2SO4
  7. 7
    浓缩concentrated under reduced pressure
  8. 8
    workup.DISTILLATIONDistillation at atmospheric pressure (170-185° C.)

实验过程

A solution of n-BuLi (83 mL, 133.0 mmol, 1.2 eq, 1.6 M in hexanes) was added to a stirred solution of 2-methylfuran (10 mL, 110.8 mmol, 1 eq) in THF (85 mL) at 0° C. under inert atmosphere. The reaction mixture was stirred for 4 h at room temperature then cooled to 0° C. Ethylene oxide (8.3 mL, 166.3 mmol, 1.5 eq) was added dropwise and the reaction mixture was allowed to warm to room temperature overnight. After quenching with saturated aqueous NH4Cl, the resulting layers were separated and the aqueous layer was extracted with Et2O (2×). The combined organic layers were dried over Na2SO4 and concentrated under reduced pressure. Distillation at atmospheric pressure (170-185° C.) gave 10.13 g (80.3 mmol, 72%) of 5-methyl-2-furanethanol (2f(2)) as a light yellow oil:

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06960474B2uspto-grants-2005_11