Reaction #1929015
ord-effd9c1ccff74051b60bd450339d0a5a
Reaction equation
water
t-BuLi
1-((E)-1,2-difluorovinyl)-4-propylcyclohexane
iodine
→
1-((Z)-1,2-difluoro-2-iodovinyl)-4-propylcyclohexane
Reagents
None
Conditions
Temperature
0°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1ExtractionThe batch is extracted with MTBE
- 2Washthe organic phase is washed with water and saturated sodium chloride solution
- 3OtherThe solution is dried
- 4Concentrationconcentrated to dryness
- 5OtherThe residue is purified by column chromatography (SiO2, pentane)
Procedure
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.