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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892225Generated: November 1, 2026

1,2-Dimethoxyethane → 3-bromo-5-[(E)-2-ethoxyvinyl]-2-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/1892225

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant3,5-Dibromo-2-(trifluoromethyl)pyridineHCID 11044942—
Reactant1-Ethoxyethene-2-boronic acid pinacol esterHCID 21973908—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product3-bromo-5-[(E)-2-ethoxyvinyl]-2-(trifluoromethyl)pyridineHCID 5940498638%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 3,5-dibromo-2-(trifluoromethyl)pyridine (1.11 g, 3.65 mmol) in water (9 mL) were added 2-[(E)-2-ethoxyvinyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.72 g, 3.65 mmol), tetrakis(triphenylphosphine)-palladium(0) (0.42 g, 0.36 mmol), 1,2-dimethoxyethane (16.7 mL), and sodium carbonate (1.16 g, 11.0 mmol). The resulting mixture was allowed to stir overnight at 60° C. After the reaction was allowed to cool to rt, EtOAc (50 mL) was added. The organic solution was separated, dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography to give 3-bromo-5-[(E)-2-ethoxyvinyl]-2-(trifluoromethyl)pyridine (0.41 g, 38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507667B2
Source datasetuspto-grants-2013_08
ORD IDord-2985cfbd46fd41d987843165f7759933
Source noteuspto-grants-2013_08