Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylvinyltin | HCID 81998 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | HCID 19603266 | HCID 19603266 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 19603510 | HCID 19603510 | 52.9% |
Reaction Steps
A mixture of 8-benzyloxy-2-methyl-4-(trifluoromethanesulfonyloxy)quinoline (300 mg), vinyltributyltin (263 mg), tetrakis(triphenylphosphine)palladium (0) (43.6 mg) and lithium chloride (96 mg) in 1,4-dioxane (6 ml) was refluxed for three hours and then left at ambient temperature overnight. The mixture was diluted with ethyl acetate and was added silica gel (70-230 mesh, 5 g) and stirred at ambient temperature for half an hour. The silica gel was removed by filtration and the filtrate was concentrated in vacuo. The residue was chromatographed on a silica gel column eluting with ethyl acetate-n-hexane (1:4, V/V) to give a solid. This solid was crystallized from diisopropyl ether to give 8-benzyloxy-2-methyl-4-vinylquinoline (110 mg) as pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05994368 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-ada9566638ee4135b30a104ff0b0b9c9 |
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| Source note | uspto-grants-1999_11 |
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