HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593422Generated: October 30, 2026
2-(Tributylstannyl)pyridine → 4-(3-Bromo-furan-2-yl)-pyridine
https://huagongshe.com/reaction/1593422
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Tributylstannyl)pyridine | HCID 607784 | — |
| Reactant | 2,3-Dibromofuran | HCID 7021501 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(3-Bromo-furan-2-yl)-pyridine | HCID 15721831 | 25% |
Reaction Steps
A solution of tributylstannylpyridine (8.0 g, 21.7 mmol) and 2,3-dibromofuran (5.9 g, 26.1 mmol) in dry toluene (200 ml) was treated with bis(triphenylphosphine)palladium (II) chloride (1.5 g, 2.2 mmol) and heated at 100° C. overnight. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate, washed with water, dried (MgSO4) and evaporated in vacuo. The residue was chromatographed on silica gel eluting with ethyl acetate to afford the title compound (1.2 g, 25%); 1H NMR (CDCl3) 8.66 (2H, d, J 11 Hz), 7.84 (2H, d, J 11 Hz), 7.50 (1H, d, J 3 Hz), 6.60 (1H, d, J 3 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07297694B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-de1c0fa68a7a4d31b1479e821a53b612 |
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| Source note | uspto-grants-2007_11 |
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