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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509715Generated: November 3, 2026

Tributylvinyltin → 5-Ethenyl-2-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/509715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
Reactant5-Bromo-2-(trifluoromethyl)pyridineHCID 2761197—
CatalystHCID 178418397HCID 178418397—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
Product5-Ethenyl-2-(trifluoromethyl)pyridineHCID 574168481,324.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

2 g of 5-bromo-2-(trifluoromethyl)pyridine was dissolved in DMF:THF (3:1, 12 mL). vinyltributyltin (3 g) and tetrakis(triphenylphosphine)palladium (135 mg) were added to this solution. The reaction mixture was degassed and purged with nitrogen for 5 min and then heated at 100° C. for 2 h. at which point the reaction was found complete (monitored by TLC). The reaction mixture was diluted with water and extracted with ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate and evaporated under reduced pressure (Caution: product may be volatile) and the residue was purified by SiO2 chromatography (100-200 mesh, eluent: hexane-ethyl acetate gradient). The requisite fractions were concentrated below 40° C. under reduced pressure to obtain 20.3 g of 2-(trifluoromethyl)-5-vinylpyridine as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096591B2
Source datasetuspto-grants-2015_08
ORD IDord-7c9bf25a03f941c39fea014dbfece14e
Source noteuspto-grants-2015_08