HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641478Generated: November 2, 2026
Bromopentafluorobenzene → HCID 54473349, compound
https://huagongshe.com/reaction/1641478
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromopentafluorobenzene | HCID 9578 | — |
| Reactant | 3-Butyn-1-OL | HCID 13566 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Catalyst | Triphenylphosphine | HCID 11776 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 54473349 | HCID 54473349 | 89.9% |
Reaction Steps
To a solution of 1-bromo-2,3,4,5,6-pentafluorobenzene (50 g) in triethylamine (200 mL), 3-butyn-1-ol (15 g), triphenylphosphine (2.7 g), dichlorobistriphenylphosphinepalladium (3.6 g) and copper (I) iodide (1.9 g) were added, followed by stirring at 80° C. for 16 hours. The reaction mixture was cooled to room temperature, and tert-butyl methyl ether (500 mL) was added thereto, followed by stirring at 0° C. for 30 minutes. The reaction mixture was filtered through “Celite” (registered trademark), and the filtrate was concentrated. The resulting residue was purified by flash column chromatography (hexane:ethyl acetate=95:5→65:35) to give the title compound (43 g) having the following physical properties.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08115014B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-dcebf366dbd94ab49f3bdcfc788b6497 |
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| Source note | uspto-grants-2012_02 |
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