HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989661Generated: October 30, 2026
3-Bromopyridine → 2-(Pyrrolidin-1-yl)pyridine
https://huagongshe.com/reaction/989661
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromopyridine | HCID 12286 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Binol | HCID 11762 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(Pyrrolidin-1-yl)pyridine | HCID 11019020 | 221.1% |
Reaction Steps
To a stirred solution of free pyrrolidine (79.3 mg; 0.22 mmol) and sodium t-butoxide (29 mg; 0.31 mmol) in dry toluene (3 mL) was added, sequentially, 3-bromopyridine (22.9 μL; 0.24 mmol), tris-(dibenzylideneacetone)dipalladium (0)(3.9 mg; cat.), and (R)-(+)-1,1′-bi-2-naphthol (5.4 mg; cat.) at room temperature under a nitrogen atmosphere. The resulting mixture was heated to 80° C., held 3 hours, then allowed to cool back to room temperature. The reaction then was diluted with ethyl acetate (40 mL), washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified via flash chromatography on silica gel (40% ethyl acetate in hexanes) to provide the N-pyridyl pyrrolidine (72.1 mg; 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06458787B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-5b6752b47faa48efb4419f73c89f9a8f |
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| Source note | uspto-grants-2002_10 |
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