تفاعل #1960495

ord-2fd8d632df444939aeb159f484faf82f

معادلة التفاعل

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

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08303844B2uspto-grants-2012_11