반응 #1960499

ord-95d931fc16054e5aac801142223e3b46

반응 방정식

CC(C)OC(=O)/N=N/C(=O)OC(C)C
DIAD
CCCC1CCC(C2CCc3cc(O)c(F)c(F)c3C2)CC1
3,4-difluoro-6-(4-propylcyclohexyl)-5,6,7,8-tetrahydronaphthalen-2-ol
C#CC(O)CCC
1-hexyn-3-ol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
C#CC(CCC)Oc1cc2c(c(F)c1F)CC(C1CCC(CCC)CC1)CC2
6-(1-ethynylbutoxy)-7,8-difluoro-2-(4-propylcyclohexyl)-1,2,3,4-tetrahydronaphthalene

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

7.0 g (22.7 mmol) of 3,4-difluoro-6-(4-propylcyclohexyl)-5,6,7,8-tetrahydronaphthalen-2-ol are initially introduced in 90 ml of THF together with 2.70 ml (24.0 mmol) of 1-hexyn-3-ol and 6.60 g (25.2 mmol) of triphenylphosphine. 5.3 ml (46.8 mmol) of DIAD in 10 ml of THF are added over the course of 20 min with ice-cooling. After 19 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-(4-propylcyclohexyl)-1,2,3,4-tetrahydronaphthalene as a colourless solid.

출처

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