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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 861407Erstellt: 24. Oktober 2026

3-(4-Bromophenyl)pyridine → 3-[2-(4-[3-Pyridyl]phenyl)ethenyl]-3-hydroxyquinuclidine

https://huagongshe.com/de/reaction/861407

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(4-Bromophenyl)pyridineHCID 1515241—
Edukt3-Ethenyl-3-hydroxy-1-azabicyclo[2.2.2]octaneHCID 22620778—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorDichlorobis(triphenylphosphine)palladiumHCID 6102075—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-[2-(4-[3-Pyridyl]phenyl)ethenyl]-3-hydroxyquinuclidineHCID 5407924129,7%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

A mixture of 3-ethenyl-3-hydroxyquinuclidine (673 mg), 3-(4-bromophenyl)pyridine (1.08 g), bis-(triphenylphosphine)-palladium (II) chloride (140 mg), copper (I) iodide (70 mg), and dimethylformamide (10 ml) was stirred at 130° C. under an atmosphere of argon for 4 hours. The mixture was evaporated and the residue was paritioned between aqueous 2M sodium hydroxide solution (10 ml) and dichloromethane (10 ml). The organic layer was separated, washed with dichloromethane (2×10 ml), dried (MgSO4) and evaporated. The residue was crystallised from acetonitrile to give 3-[2-(4-[3-pyridyl]phenyl)ethenyl]-3-hydroxyquinuclidine (400 mg) as a solid, m.p. 195°-198° C.; microanalysis, found: C, 76.4; H, 7.2; N, 8.6%; C20H22N2O.0.5H2O requires: C, 76.2; H, 7.3; N, 8.9%; NMR (DMSO-d6 +CD3COOD): 1.7-2.15(4H, m), 2.35(1H, m), 3.15-3.4(5H, m), 3.5(1H, d), 6.7(1H, d), 6.9(1H, d), 7.5-7.8(7H, m), 8.15(1H, d); m/Z 307 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05714496
Quelldatensatzuspto-grants-1998_02
ORD IDord-7e48db0894324707a0c7c9d3c3b3308f
Quellennotizuspto-grants-1998_02