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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72103Generated: October 26, 2026

1-Bromo-2-fluorobenzene → 5-(2-Fluorophenyl)pent-4-yn-1-ol

https://huagongshe.com/reaction/72103

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-fluorobenzeneHCID 61259—
Reactant4-Pentyn-1-olHCID 79346—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventAcetonitrileHCID 6342—
Product5-(2-Fluorophenyl)pent-4-yn-1-olHCID 86687856—

Reaction Steps

1-Bromo-2-fluorobenzene [1072-85-1] (3.0 g, 17 mmol, 1.0 equiv) and pent-4-yn-1-ol [5390-04-5] (2.3 mL, 25 mmol, 1.5 equiv) were dissolved in acetonitrile (40 mL). CuI (0.13 g, 0.68 mmol, 0.04 equiv) and TEA (3.4 mL, 25 mmol, 1.5 equiv) was added to the stirred solution followed by tetrakis(triphenylphosphine)palladium(0) (0.39 g, 0.34 mmol, 0.02 equiv). The solution was heated at reflux for 16 hours. The solution was cooled, filtered through Celite, the Celite pad rinsed with EtOAc and the solvent removed by rotoevaporation. Column chromatography (9:1 hexanes:ethyl acetate) of the residue afforded pure 5-(2-fluorophenyl)pent-4-yn-1-ol Intermediate 60 (1.3 g, 43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828973B2
Source datasetuspto-grants-2014_09
ORD IDord-aba1e866d2cd413daa1a31e8afd20c22
Source noteuspto-grants-2014_09