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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510045Generated: November 2, 2026

1-Bromo-4-iodobenzene → 4-[1-(4-Bromophenyl)piperidin-4-yloxy]pyridine

https://huagongshe.com/reaction/1510045

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-iodobenzeneHCID 11522—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant4-(Piperidin-4-yloxy)pyridineHCID 5152155—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product4-[1-(4-Bromophenyl)piperidin-4-yloxy]pyridineHCID 6686331650.9%

Reaction Conditions

Temperature110 °C

Reaction Steps

2 g of 1-bromo-4-iodobenzene and 1.386 g of 4-(piperidin-4-yloxy)pyridine are placed in 35 ml of toluene and then 0.324 g of tris(dibenzylideneacetone)dipalladium(0), 0.245 g of 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene and 1.019 g of sodium tert-butoxide are added. The reaction medium is heated at 110° C. for 18 h. Ethyl acetate is subsequently added and the mixture is washed twice with water and once with a saturated aqueous sodium chloride solution. The organic phase is dried over magnesium sulphate and concentrated under reduced pressure. The crude product obtained is chromatographed on silica gel, elution being carried out with a gradient of a dichloromethane/methanol (99/1 to 98/2) mixture. 1.2 g of 4-[1-(4-bromophenyl)piperidin-4-yloxy]pyridine are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211892B2
Source datasetuspto-grants-2012_07
ORD IDord-5ab70dd6b78b42018b1fb625cdcd2184
Source noteuspto-grants-2012_07