HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207030Generated: November 1, 2026
Tributylvinyltin → 5-Bromo-2,7-dimethyl-6-vinylquinoline
https://huagongshe.com/reaction/2207030
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributylvinyltin | HCID 81998 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 5-Bromo-2,7-dimethylquinolin-6-yl trifluoromethanesulfonate | HCID 86691977 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Bromo-2,7-dimethyl-6-vinylquinoline | HCID 66631391 | — |
Reaction Steps
PdCl2(PPh3)2 (207 mg, 0.30 mmol) were added to a mixture 5-bromo-2,7-dimethylquinolin-6-yl trifluoromethanesulfonate (1.13 g, 2.95 mmol), tributyl-vinyl-stannane (0.95 mL, 3.25 mmol), lithium chloride (375 mg, 8.85 mmol) in DMF (30 mL). The reaction mixture was flushed with nitrogen, heated at 80° C. for 4 hours, cooled to room temperature. The mixture was diluted by ethyl acetate, washed with NaHCO3 solution, water and brine, dried over Na2SO4, filtered and concentrated in vacuo. The obtained residue was purified by flash chromatography to provide the desired product. LCMS-ESI+: calc'd for C13H12BrN: 262.0 (M+H+); Found: 262.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376392B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-4ee15febd3ec48f5aeaec4c0a4e4d97d |
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| Source note | uspto-grants-2016_06 |
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