Реакция #1929015

ord-effd9c1ccff74051b60bd450339d0a5a

Уравнение реакции

O
water
[Li][C](C)(C)C
t-BuLi
CCCC1CCC(/C(F)=C\F)CC1
1-((E)-1,2-difluorovinyl)-4-propylcyclohexane
II
iodine
CCCC1CCC(/C(F)=C(\F)I)CC1
1-((Z)-1,2-difluoro-2-iodovinyl)-4-propylcyclohexane

Растворители

Условия реакции

Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ЭкстракцияThe batch is extracted with MTBE
  2. 2
    Промывкаthe organic phase is washed with water and saturated sodium chloride solution
  3. 3
    ДругоеThe solution is dried
  4. 4
    Концентрированиеconcentrated to dryness
  5. 5
    ДругоеThe residue is purified by column chromatography (SiO2, pentane)

Методика

7.0 g (26.3 mmol) of 1-((E)-1,2-difluorovinyl)-4-propylcyclohexane are initially introduced in 150 ml of THF at −55° C., and 20.5 ml (30.2 mmol, 15% soln. in n-pentane) of t-BuLi are metered in. After 2 h at this temperature, a solution of 7.67 g (30.0 mmol) of iodine in 50 ml of THF is added dropwise. The mixture is slowly warmed to 0° C., and water is added. The batch is extracted with MTBE, and the organic phase is washed with water and saturated sodium chloride solution. The solution is dried using sodium sulfate and concentrated to dryness. The residue is purified by column chromatography (SiO2, pentane), giving 1-((Z)-1,2-difluoro-2-iodovinyl)-4-propylcyclohexane as a pale-violet oil.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08945420B2uspto-grants-2015_02