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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841833Generated: November 1, 2026

Iodine → 1-((Z)-1,2-difluoro-2-iodovinyl)-4-propylcyclohexane

https://huagongshe.com/reaction/1841833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantWaterHCID 962—
ReactantHCID 67328702HCID 67328702—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Product1-((Z)-1,2-difluoro-2-iodovinyl)-4-propylcyclohexaneHCID 86674303—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08945420B2
Source datasetuspto-grants-2015_02
ORD IDord-effd9c1ccff74051b60bd450339d0a5a
Source noteuspto-grants-2015_02