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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1335721Generated: October 29, 2026

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

https://huagongshe.com/reaction/1335721

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromopyridineHCID 12286—
Reactant4-PhenylpiperidineHCID 69873—
ReagentSodium trimethylsilanolateHCID 23672319—
CatalystNickel(II) iodideHCID 26038—
Catalyst2-((2,6-Dimethoxyphenyl)amino)-2-oxoacetic acidHCID 118864503—
SolventDimethyl SulfoxideHCID 679—
ProductCaffeineHCID 2519—
Product3-(4-Phenyl-1-piperidinyl)pyridineHCID 1223802231.611%
Product4-(4-Phenylpiperidin-1-yl)pyridineHCID 1398883372.037%

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-1db4ed1380b447708a30aa5c2c4afc70
Source noteHigh-throughput exploration of 50,688 Pd-, Ni- and Cu-catalysed C–N coupling reactions