반응 #1960495

ord-2fd8d632df444939aeb159f484faf82f

반응 방정식

CCCCCC1CCc2cc(O)c(F)c(F)c2O1
7,8-difluoro-2-pentylchroman-6-ol
C#CC(O)CCC
1-hexyn-3-ol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CC(C)OC(=O)/N=N/C(=O)OC(C)C
DIAD
C#CC(CCC)Oc1cc2c(c(F)c1F)OC(CCCCC)CC2
6-(1-ethynylbutoxy)-7,8-difluoro-2-pentylchroman

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONare added over the course of 20 min with ice-
  2. 2
    온도cooling
  3. 3
    추출the mixture is extracted a number of times with MTBE
  4. 4
    세척The combined organic phases are washed with water and saturated sodium chloride soln
  5. 5
    기타, and the solution is dried
  6. 6
    기타after removal of the solvents
  7. 7
    기타is purified by column chromatography (SiO2, n-heptane:MTBE=2:1)

실험 절차

10.0 g (39.0 mmol) of 7,8-difluoro-2-pentylchroman-6-ol are initially introduced in 140 ml of THF together with 4.0 g (41.0 mmol) of 1-hexyn-3-ol and 11.3 g (42.9 mmol) of triphenylphosphine, and 9.1 ml (46.8 mmol) of DIAD are added over the course of 20 min with ice-cooling. After 18 h at RT, water 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 soln., and the solution is dried using sodium sulfate. The residue remaining after removal of the solvents is purified by column chromatography (SiO2, n-heptane:MTBE=2:1), giving 6-(1-ethynylbutoxy)-7,8-difluoro-2-pentylchroman as a yellow oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08303844B2uspto-grants-2012_11