Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672235Generated: October 30, 2026

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

https://huagongshe.com/reaction/1672235

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 numberUS07998952B2
Source datasetuspto-grants-2011_08
ORD IDord-42e49160b0a546f4be4444a2cd0212d2
Source noteuspto-grants-2011_08