HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395941Generated: October 30, 2026
1-Bromo-4-fluorobenzene → 4-(4-Fluorophenyl)but-3-yn-1-ol
https://huagongshe.com/reaction/2395941
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Butyn-1-OL | HCID 13566 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 4-(4-Fluorophenyl)but-3-yn-1-ol | HCID 12478440 | 86% |
Reaction Steps
1 g of bis-(triphenylphosphine)-palladium(II) chloride, 3.8 g of copper(I) iodide and 8.7 g of triphenylphosphine were added in succession to a solution of 100 g of 4-bromofluorobenzene in 350 ml of triethylamine. The mixture was heated to reflux temperature, after which 43.4 g of 3-butynol were added dropwise in the course of 20 minutes at this temperature (about100° C.). Stirring was carried out for a further 5 hours at this temperature. After the mixture had cooled, the triethylamine was distilledoff. The residue was taken up in methyl tert-butyl ether and water. The aqueous phase was extracted twice more with methyl tert-butyl ether, and the combined organic extracts were washed in succession with 1 N hydrochloric acid and with 10% strength by weight sodium bicarbonate solution and dried over sodium sulfate. After removal of the solvent, the crude product was distilled under greatly reduced pressure. Yield: 86%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05491123 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-d9acc85bdca047c7b337418bf2c35785 |
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| Source note | uspto-grants-1996_02 |
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