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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantTriphenylphosphineHCID 11776—
Reactant3-Butyn-1-OLHCID 13566—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
Solventtert-Butyl methyl etherHCID 15413—
Product4-(4-Fluorophenyl)but-3-yn-1-olHCID 1247844086%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05491123
Source datasetuspto-grants-1996_02
ORD IDord-d9acc85bdca047c7b337418bf2c35785
Source noteuspto-grants-1996_02