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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471156Generated: October 31, 2026

Stannane, tributyl(1-ethoxyethenyl)- → 6-Bromo-2-(1-ethoxyvinyl)quinoxaline

https://huagongshe.com/reaction/1471156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
Reactant6-Bromo-2-chloroquinoxalineHCID 12686408—
CatalystHCID 178418476HCID 178418476—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
Product6-Bromo-2-(1-ethoxyvinyl)quinoxalineHCID 5849876352.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

Dichlorobis(triphenylphosphine)-palladium(II) (17.30 mg, 0.025 mmol) was added to a solution of 6-bromo-2-chloroquinoxaline (60 mg, 0.246 mmol) and tributyl(1-ethoxyvinyl)stannane (107 mg, 0.296 mmol) in dioxane (1.5 mL) and the mixture was stirred at 110° C. for 2 h. The reaction was diluted with MeOH, and purified by prep HPLC (H2O-MeOH with 10 mM NH4OAc buffer) to yield 6-bromo-2-(1-ethoxyvinyl)quinoxaline (36 mg, 0.129 mmol, 52.3% yield) as white solid. LC-MS retention time 2.76 min; m/z 279 [M+H]+. (Column PHENOMENEX® Luna 3.0×50 mm S10. Solvent A=90% water:10% methanol:0.1% TFA. Solvent B=10% water:90% methanol:0.1% TFA. Flow Rate=4 mL/min. Start % B=0. Final % B=100. Gradient Time=3 min. Wavelength=220).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006455B2
Source datasetuspto-grants-2015_04
ORD IDord-1b76c516b3a94445a30dcb1195ad5d60
Source noteuspto-grants-2015_04