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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1338004Generated: November 1, 2026

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

https://huagongshe.com/reaction/1338004

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromopyridineHCID 12286—
Reactant4-PhenylpiperidineHCID 69873—
ReagentPotassium tert-butoxideHCID 23665647—
Catalystcopper(I) bromideHCID 24593—
CatalystBis(adamantan-1-yl)(butyl)phosphaneHCID 11371790—
SolventDimethyl SulfoxideHCID 679—
ProductCaffeineHCID 2519—
Product3-(4-Phenyl-1-piperidinyl)pyridineHCID 12238022323.613%
Product4-(4-Phenylpiperidin-1-yl)pyridineHCID 13988833724.073%

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-ec032852799e481a86754cb62d14e81d
Source noteHigh-throughput exploration of 50,688 Pd-, Ni- and Cu-catalysed C–N coupling reactions