反应 #1960487

ord-918c2e9f0685481898db33b3d2ac659d

反应方程式

Oc1cc2c(c(F)c1F)OCCC2
7,8-difluorochroman-6-ol
C#CC(O)C1CCC(CCC)CC1
1-(4-propylcyclohexyl)-prop-2-yn-1-ol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CC(C)OC(=O)/N=N/C(=O)OC(C)C
DIAD
[Cl-].[Na+]
sodium chloride
C#CC(Oc1cc2c(c(F)c1F)OCCC2)C1CCC(CCC)CC1
7,8-difluoro-6-[1-(4-propylcyclohexyl)prop-2-ynyloxy]chroman

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONare added over the course of 30 min with ice-
  2. 2
    温度cooling
  3. 3
    萃取the mixture is extracted a number of times with MTBE
  4. 4
    洗涤The combined organic phases are washed with water and saturated sodium chloride solution
  5. 5
    其他the solution is dried
  6. 6
    其他after removal of the solvents
  7. 7
    其他is purified by column chromatography (SiO2, n-pentane:MTBE=2:1)

实验过程

5.0 g (26.9 mmol) of 7,8-difluorochroman-6-ol are initially introduced in 65 ml of THF together with 5.33 g (29.6 mmol) of 1-(4-propylcyclohexyl)-prop-2-yn-1-ol and 8.45 g (32.2 mmol) of triphenylphosphine, and 6.79 ml (34.9 mmol) of DIAD are added over the course of 30 min with ice-cooling. After 19 h at RT, semi-saturated sodium chloride solution is added, and the mixture is extracted a number of times with MTBE. The combined organic phases are washed with water and saturated sodium chloride solution, and the solution is dried using sodium sulfate. The residue remaining after removal of the solvents is purified by column chromatography (SiO2, n-pentane:MTBE=2:1), giving 7,8-difluoro-6-[1-(4-propylcyclohexyl)prop-2-ynyloxy]chroman as a pale-brown oil.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08303844B2uspto-grants-2012_11