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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234874Generated: October 30, 2026

1-Bromo-4-fluorobenzene → 4-(4-Fluorophenyl)but-3-yn-1-ol

https://huagongshe.com/reaction/234874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantTriphenylphosphineHCID 11776—
Reactant3-Butyn-1-OLHCID 13566—
CatalystCopper iodideHCID 83717—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTriethylamineHCID 8471—
Product4-(4-Fluorophenyl)but-3-yn-1-olHCID 1247844086%

Reaction Steps

1 g of bis(triphenylphosphine)-palladium(II)-chloride, 3.8 g of copper(II)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. This mixture was heated to the reflux temperature, after which 43.4 g of 3-butynol were added dropwise in the course of 20 minutes at this temperature (about 100° C.). Stirring was continued for a further 5 hours at this temperature. After cooling, the triethylamine was distilled off. The residue was taken up in methyl tertbutyl 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 1N hydrochloric acid and with 10% strength sodium bicarbonate solution and was 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 numberUS05597776
Source datasetuspto-grants-1997_01
ORD IDord-62f202c0015d48d4bf019b80b7a4e265
Source noteuspto-grants-1997_01