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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501952Generated: November 2, 2026

Potassium vinyltrifluoroborate → HCID 66643894, compound

https://huagongshe.com/reaction/1501952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium vinyltrifluoroborateHCID 23679353—
ReactantHCID 66819934HCID 66819934—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 66643894HCID 66643894—

Reaction Conditions

Temperature60 °C

Reaction Steps

4,5-Dibromo-2-benzofuran-1(3H)-one (3.00 g, 10.3 mmol), Potassium vinyltrifluoroborate (12.7 g, 20.6 mmol) and Pd(dppf)Cl2 (839 mg, 1.03 mmol) in TEA (2.7 mL) and EtOH (15 mL) were added to a flask containing a stir bar. The flask was then heated at 60° C. for 2 h. TLC showed clean and complete reaction. The organic residue was dissolved in EtOAc (500 mL) and the solution was washed with brine, dried over sodium sulfate, filtered and concentrated. The resulting organic residue was subjected to purification over silica gel to give 4-bromo-5-ethenyl-2-benzofuran-1(3H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206199B2
Source datasetuspto-grants-2015_12
ORD IDord-b043cc21a0d742ca871442f860401d14
Source noteuspto-grants-2015_12