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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 67328702 | HCID 67328702 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-((Z)-1,2-difluoro-2-iodovinyl)-4-propylcyclohexane | HCID 86674303 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08945420B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-effd9c1ccff74051b60bd450339d0a5a |
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| Source note | uspto-grants-2015_02 |
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