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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 72103Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/72103

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-2-fluorobenzeneHCID 61259—
Edukt4-Pentyn-1-olHCID 79346—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelAcetonitrileHCID 6342—
Produkt5-(2-Fluorophenyl)pent-4-yn-1-olHCID 86687856—

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08828973B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-aba1e866d2cd413daa1a31e8afd20c22
Quellennotizuspto-grants-2014_09