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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1337780Generated: November 1, 2026

3-Bromopyridine → 4-(4-Phenylpiperidin-1-yl)pyridine

https://huagongshe.com/reaction/1337780

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromopyridineHCID 12286—
Reactant4-PhenylpiperidineHCID 69873—
ReagentPotassium tert-butoxideHCID 23665647—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Catalyst4,4'-Bi-1,3-benzodioxole-5,5'-diylbis{bis[4-methoxy-3,5-bis(2-methyl-2-propanyl)phenyl]phosphine}HCID 11194192—
SolventDimethyl SulfoxideHCID 679—
ProductCaffeineHCID 2519—
Product3-(4-Phenyl-1-piperidinyl)pyridineHCID 12238022322.341%
Product4-(4-Phenylpiperidin-1-yl)pyridineHCID 13988833722.36%

Reaction Conditions

Temperature60 °C

Provenance & Evidence

DOI10.1021/jacs.6c05959
Source datasetHigh-throughput exploration of 50,688 Pd-, Ni- and Cu-catalysed C–N coupling reactions
ORD IDord-4edaea290f1543cf9b8bc9554ab12d27
Source noteHigh-throughput exploration of 50,688 Pd-, Ni- and Cu-catalysed C–N coupling reactions