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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678018Generated: November 1, 2026

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

https://huagongshe.com/reaction/1678018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPyrrolidineHCID 31268—
Reactant1,4-DibromonaphthaleneHCID 66521—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product1-(4-Bromo-1-naphthyl)pyrrolidineHCID 66798110—

Reaction Conditions

Temperature70 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008307B2
Source datasetuspto-grants-2011_08
ORD IDord-7ae568e26b494980a2cca13d4fc207a6
Source noteuspto-grants-2011_08