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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-(5-Bromopyridin-2-yl)piperazine | HCID 16414227 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Benzyl Alcohol | HCID 244 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[5-(Benzyloxy)pyridin-2-yl]piperazine | HCID 22221504 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07485644B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-41f8b5fb1c31496a9f2284f859b4286d |
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| Source note | uspto-grants-2009_02 |
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