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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 447689Erstellt: 24. Oktober 2026

Toluene → 1-(4-Bromo-1-naphthyl)pyrrolidine

https://huagongshe.com/de/reaction/447689

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktPyrrolidineHCID 31268—
Edukt1,4-DibromonaphthaleneHCID 66521—
EduktBinap, (A+-)-HCID 634876—
EduktSodium t-butoxideHCID 23676156—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
Produkt1-(4-Bromo-1-naphthyl)pyrrolidineHCID 66798110—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

To a solution of 1,4-dibromonaphthalene (500 mg, 0.002 mol), Pyrrolidine (0.18 mL, 0.0021 mol), (R)-(+)-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl (0.022 g, 0.000035 mol), Sodium tert-butoxide (0.24 g, 0.0024 mol) in Toluene (5.00 mL, 0.0469 mol) was added Tris(dibenzylideneacetone)dipalladium(0) (0.008 g, 0.000009 mol), and the mixture was heated at 70° C. overnight. The reaction was cooled, quenched by addition of water and the mixture was extracted with DCM (3×), washed with water, brine, dried (Na2SO4), filtered and concentrated. The residue was purified by flash chromatography (0 to 25% hexanes/DCM) to obtain 400 mg (80%). Reference: Jean, L.; Rouden, J.; Maddaluno, J.; Lasne, M-C. J. Org. Chem. 2004, 69, 8893-8902.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08481550B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-9bb90f02c0ef4097825062ccacdf1a66
Quellennotizuspto-grants-2013_07