HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436105Generated: November 3, 2026
Hexane → 1,2,3-trifluoro-5-((E)-propenyl)benzene
https://huagongshe.com/reaction/1436105
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexane | HCID 8058 | — |
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | 1-Bromo-3,4,5-trifluorobenzene | HCID 611409 | — |
| Reactant | ((1E)-prop-1-en-1-yl)boronic acid | HCID 6157276 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1,2,3-trifluoro-5-((E)-propenyl)benzene | HCID 68716515 | 84.1% |
Reaction Steps
Tetrakistriphenylphosphine palladium (0) (4.66 g) and cesium fluoride (21.4 g) were added to a solution of 1-bromo-3,4,5-trifluorobenzene (8.5 g) and trans-1-propen-1-ylboronic acid (4.1 g) in dioxane (95 ml) and water (5 ml) in a nitrogen atmosphere, and the reaction solution was stirred at 80° C. for five hours. The reaction solution was returned to room temperature. Then, hexane and water were added to the reaction solution, and the insoluble matter was removed by filtration. The organic layer was separated and then washed with water, and the insoluble matter was removed by filtration again. The organic layer was separated and then sequentially washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (hexane) to obtain 5.83 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07618960B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-22356bfd4e4744c38fc19a635aea4604 |
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| Source note | uspto-grants-2009_11 |
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