HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217599Generated: October 29, 2026
2,5-Dibromopyridine → 5-Bromo-2-(3-methoxy-prop-1-ynyl)-pyridine
https://huagongshe.com/reaction/217599
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Reactant | 3-Methoxypropyne | HCID 69393 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Bromo-2-(3-methoxy-prop-1-ynyl)-pyridine | HCID 22503261 | 59.6% |
Reaction Steps
A solution of 2,5-dibromo-pyridine (41, 4.64 g, 19.6 mmol), 3-methoxy-propyne (30, 1.66 mL, 19.7 mmol), and copper(I) iodide (0.084 g, 0.44 mmol) in 61.6 mL of triethylamine was purged with nitrogen, and bis(triphenylphosphine)palladium(II) chloride (0.31 g, 0.44 mmol) was added at 0° C. The resulting mixture was stirred at 0° C. for 1 hour, then at room temperature for 1 hour. The reaction mixture was diluted with ethyl acetate, then washed with water and brine. The organic layer was dried with anhydrous sodium sulfate, filtered and the filtrate concentrated under vacuum. The crude material was purified by silica gel flash chromatography eluting with ethyl acetate and hexane. The appropriate fractions were combined and the solvents removed under vacuum to provide the desired compound (42, 2.64 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08198273B2 |
|---|
| Source dataset | uspto-grants-2012_06 |
|---|
| ORD ID | ord-e3b5e0cbec874752834aaf1c6e5f504c |
|---|
| Source note | uspto-grants-2012_06 |
|---|