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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481373Generated: October 30, 2026

5-Bromo-1-methylpyridin-2(1H)-one → HCID 68559883, compound

https://huagongshe.com/reaction/1481373

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-1-methylpyridin-2(1H)-oneHCID 13024027—
ReactantTri(butyl)vinyltinHCID 53438229—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68559883HCID 68559883746.1%

Reaction Steps

The title compound was prepared by following general procedure 2. To a solution of 5-bromo-1-methylpyridin-2(1H)-one (2 g, 10.63 mmol) in 20 mL of 1,4-dioxane, dichlorobis(triphenylphosphine)palladium(II) (0.834 g, 1.19 mmol) was added at RT and stirred at the same temperature for 5 min. Tributylvinyltin (3.46 mL, 1.19 mmol) was added slowly at RT and stirred at 100-105° C. for 2 h. The reaction was monitored by TLC and LCMS. After completion of the starting material, the solvent was evaporated and the residue purified by column chromatography using 60% ethyl acetate-hexane to afford 1.2 g of 1-methyl-5-vinylpyridin-2(1H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409910B2
Source datasetuspto-grants-2016_08
ORD IDord-2feb935625cc4347a61bde679f90dd80
Source noteuspto-grants-2016_08