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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810220Generated: October 26, 2026

1-Bromo-4-iodobenzene → 4-Benzyl-1-(4-bromophenyl)piperidine

https://huagongshe.com/reaction/1810220

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-iodobenzeneHCID 11522—
Reactant1,1'-BinaphthylHCID 11789—
Reactant4-BenzylpiperidineHCID 31738—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
Product4-Benzyl-1-(4-bromophenyl)piperidineHCID 12169538—

Reaction Steps

A mixture of 1-bromo-4-iodo benzene (0.500 g), 4-benzylpiperidine (0.25 mL), sodium-tert-butylate (0.238 g), tris(dibenzylideneacetone)dipalladium (0.016 g) and 2,2′-bis/diphenylphosphino)-1,1′-binaphtyl racemate (0.018 g) is dissolved in tetrahydrofuran and stirred at room temperature overnight. The reaction mixture is concentrated and the resulting residue is loaded on Celite and purified by silica gel chromatography (4:1 hexanes/ethyl acetate) to give 4-benzyl-1-(4-bromo-phenyl)-piperidine as a light yellow syrup. MS (m/z): 331 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362063B2
Source datasetuspto-grants-2013_01
ORD IDord-ecf5b55f8fb3448d90604dd39b9dbcf3
Source noteuspto-grants-2013_01