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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1340302Generated: October 30, 2026

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

https://huagongshe.com/reaction/1340302

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromopyridineHCID 12286—
Reactant4-PhenylpiperidineHCID 69873—
ReagentPotassium tert-butoxideHCID 23665647—
Catalyst2-((2,6-Dimethoxyphenyl)amino)-2-oxoacetic acidHCID 118864503—
CatalystHCID 178486304HCID 178486304—
SolventDimethyl SulfoxideHCID 679—
ProductCaffeineHCID 2519—
Product3-(4-Phenyl-1-piperidinyl)pyridineHCID 12238022318.548%
Product4-(4-Phenylpiperidin-1-yl)pyridineHCID 13988833719.012%

Reaction Conditions

Temperature30 °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-d76f98cc91d347d6b0be05eecd7ef11f
Source noteHigh-throughput exploration of 50,688 Pd-, Ni- and Cu-catalysed C–N coupling reactions