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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481369Generated: October 31, 2026

Tributylvinyltin → Methyl 5-ethenylpyridine-2-carboxylate

https://huagongshe.com/reaction/1481369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
ReactantMethyl 5-bromopyridine-2-carboxylateHCID 7016458—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 5-ethenylpyridine-2-carboxylateHCID 5741684566.3%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409910B2
Source datasetuspto-grants-2016_08
ORD IDord-7f9c8f6ea5c84d1b928d26cf891a4e6f
Source noteuspto-grants-2016_08