HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045526Generated: November 1, 2026
Tributylvinyltin → Methyl 5-ethenylpyridine-2-carboxylate
https://huagongshe.com/reaction/1045526
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributylvinyltin | HCID 81998 | — |
| Reactant | Methyl 5-bromopyridine-2-carboxylate | HCID 7016458 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 5-ethenylpyridine-2-carboxylate | HCID 57416845 | 66.3% |
Reaction Steps
The title compound was prepared by following general procedure 2. Methyl 5-bromopyridine-2-carboxylate (4.0 g, 18.5 mmol) was dissolved in 160 mL dioxane. Vinyltributyltin (11.7 g, 37 mmol) was added to this solution at 25° C., followed by addition of dichlorobis(triphenylphosphine) palladium (1.5 g, mmol). The reaction mixture was degassed and purged with nitrogen for 5 min. and then heated at 100° C. for 2 h. The reaction mixture was evaporated under reduced pressure and the residue was purified by SiO2 chromatography (100-200 mesh, eluent: hexane-50% ethyl acetate-hexane gradient). The requisite fractions were concentrated below 40° C. under reduced pressure to obtain 2 g of methyl 5-vinylpyridine-2-carboxylate as a pale yellow oil (solid at −20° C.). TLC Rf 0.3 in 40% Ethyl acetate:Hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569287B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-6864eb6c3bcb432f85c0e2e75862f2e2 |
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| Source note | uspto-grants-2013_10 |
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