HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931746Generated: November 1, 2026
Tributylvinyltin → 5-Bromo-7-methyl-6-vinylquinoline
https://huagongshe.com/reaction/931746
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributylvinyltin | HCID 81998 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 5-Bromo-7-methylquinolin-6-yl trifluoromethanesulfonate | HCID 86691979 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Bromo-7-methyl-6-vinylquinoline | HCID 66630662 | 78% |
Reaction Steps
A mixture of 5-bromo-7-methylquinolin-6-yl trifluoromethanesulfonate (230 mg, 0.62 mmol), tributyl(vinyl)stannane (200 μL, 0.68 mmol), lithium chloride (78 mg, 1.86 mmol) and PdCl2(PPh3)2 (43 mg) in DMF (10 mL) was heated at 80° C. for 16 hours, and then the volatile component was removed in vacuo. The residue was dissolved in ethyl acetate (100 mL), washed with NaHCO3 solution, water and brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography (hexanes/EtOAc) to provide 5-bromo-7-methyl-6-vinylquinoline (120 mg). LCMS-ESI+ (m/z): 248.2, 250.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296758B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-8703117344c54ace8062b9a4eca4b2be |
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| Source note | uspto-grants-2016_03 |
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