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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723810Generated: November 2, 2026

1,10-Phenanthroline → 1-[5-(Benzyloxy)pyridin-2-yl]piperazine

https://huagongshe.com/reaction/1723810

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,10-PhenanthrolineHCID 1318—
ReactantCesium carbonateHCID 10796—
Reactant1-(5-Bromopyridin-2-yl)piperazineHCID 16414227—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventBenzyl AlcoholHCID 244—
SolventDichloromethaneHCID 6344—
Product1-[5-(Benzyloxy)pyridin-2-yl]piperazineHCID 22221504—

Reaction Conditions

Temperature120 °C

Reaction Steps

A vigorously stirred suspension of 1-(5-bromopyridin-2-yl)piperazine (CAS number 73406-97-0, 116 g, 479 mmol), 1,10-phenanthroline (17.3 g, 96 mmol), Cesium carbonate (312 g, 960 mmol) and Copper (I) iodide (91 g, 480 mmol) in benzyl alcohol (960 mL) was stirred at 120° C. under an inert atmosphere for 24 hours, adding further aliquots of copper (I) iodide (5×91 g) every hour. Cooled to 40° C. and diluted with DCM (1L), stirring at room temperature for 30 minutes. Filtered through celite, washing well with DCM (500 mL). The fractions were washed with NaOH (2M, 300 mL), combined and extracted with HCl (2M, 5×1L). The combined acidic extracts were washed with DCM (500 mL), cooled to 0° C. and extracted into DCM (1L), basifying slowly with NaOH (˜46 wt %) to pH10. The aqueous layer was further extracted with DCM (2×500 mL) and the volatiles removed in vacuo, to give 1-[5-(benzyloxy)pyridin-2-yl]piperazine as a black liquor (104 g, 278 mmol @ 72 wt %, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485644B2
Source datasetuspto-grants-2009_02
ORD IDord-41f8b5fb1c31496a9f2284f859b4286d
Source noteuspto-grants-2009_02